2-Methylactonitrile

2-Tone music

2-P

2-Oleoylglycerol

2-amino-1-hydroxybenzene

2-Methylenepentanedinitrile

2-Pyrrolidone is an organic compound consisting of a 5-membered lactam, making it the simplest γ-lactam. It is a colorless liquid that is miscible with water and most common organic solvents. It is produced industrially by treating butyrolactone with ammonia. Alternative routes include the partial hydrogenation of succinimide and the carbonylation of allylamine with methyl amine. 2-Pyrrolidone is an intermediate in the production of vinylpyrrolidone and the drug piracetam.

2-Nitrophenyl-b-D-galactopyranoside

2-Pyridin-2-ylethanamine

2-Phenylethylbromide is an organobromide that can be produced by the action of bromine and red phosphorus on 2-phenylethanol. It is moderately toxic by ingestion. When reacted with hydrazine, phenelzine is produced.

o-Nitrobenzaldehyde

2-Nitrovinylbenzene

In enzymology, a 2-acylglycerol O-acyltransferase (EC 2.3.1.22) is an enzyme that catalyzes the chemical reaction acyl-CoA + 2-acylglycerol CoA + diacylglycerol Thus, the two substrates of this enzyme are acyl-CoA and , whereas its two products are CoA and diacylglycerol.

2-Octyl cyanoacrylate is a cyanoacrylate ester typically used as a wound closure adhesive (under the brand name Dermabond). It is closely related to octyl cyanoacrylate.

2-W

2-Nonenal is an unsaturated aldehyde. The colorless liquid is an important aroma component of aged beer and buckwheat.

2-Methylheptane

2-Naphthol, or β-naphthol, is a fluorescent colorless (or occasionally yellow) crystalline solid with the formula C10H7OH. It is an isomer of 1-naphthol, differing by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol, but more reactive. Both isomers are soluble in simple alcohols, ethers, and chloroform. 2-Naphthol is a widely used intermediate for the production of dyes and other compounds.

2-Pyrrolidone

2-Methylbutyryl-CoA is an intermediate in the metabolism of isoleucine.

[1,1'-Biphenyl]-2-ol

2-Nitrobenzoic acid

α-Pyrone

2-Z is an album by American jazz pianist Matthew Shipp with AACM saxophonist Roscoe Mitchell, which was recorded in 1995 and released on the 2.13.61 label. Shipp played previously with Mitchell's Note Factory on the album This Dance Is for Steve McCall, but 2-Z represents their first collaboration with Shipp as a leader.

2-amino-1,3-thiazole

2-Methylimidazole is an organic compound that is structurally related to imidazole with the chemical formula CH3C3H2N2H. It is a white or colorless solid that is highly soluble in polar organic solvents and water. It is a precursor to a range of drugs and is a ligand in coordination chemistry.

This page provides supplementary chemical data on 2-pyridone.

2-Methylbutyryl-CoA dehydrogenase deficiency, is an autosomal recessive metabolic disorder. It causes the body to be unable to process the amino acid isoleucine properly. Initial case reports identified individuals with developmental delay and epilepsy, however most cases identified through newborn screening have been asymptomatic.

2-Venn diagram

2-Methyl-THF

2-Phenylphenol

2-Methylpentan-1-ol

2-Vinylpyridine

2-Pentyne

2-Propylheptanol (2PH) is a colourless waxy or oily solid.

2-Propenol

2-Phenethyl bromide

2-Methylpyridine, or 2-picoline, is the compound described with formula C6H7N. 2-Picoline is a colorless liquid that has an unpleasant odor similar to pyridine. It is mainly used to make vinylpyridine and the agrichemical nitrapyrin.

(S-[2-[3-[[4-[[[5-(6-Aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethyl] 2-methyl-3-oxobutanethioate)

2-Methyl-6-(phenylethynyl)pyridine

Non-2-enal

2-polyprenyl-6-hydroxyphenyl methylase (EC 2.1.1.222, ubiG (gene), ubiG methyltransferase, 2-octaprenyl-6-hydroxyphenyl methylase) is an enzyme with systematic name S-adenosyl-L-methionine:3-(all-trans-polyprenyl)benzene-1,2-diol 2-O-methyltransferase. This enzyme catalyses the following chemical reaction S-adenosyl-L-methionine + 3-(all-trans-polyprenyl)benzene-1,2-diol S-adenosyl-L-homocysteine + 2-methoxy-6-(all-trans-polyprenyl)phenol UbiG catalyses both methylation steps in ubiquinone biosynthesis in Escherichia coli.

2-Ocean Navy Act

1-methyl-2-nitro-benzene

2-Way

2-XL robot

2-Methylpropenenitrile

Pentan-2-one

2-Methyl phenol

2,5-dimethoxy-4-nitroamphetamine

2-Phosphoglyceric acid (2PG), or 2-phosphoglycerate, is a glyceric acid which serves as the substrate in the ninth step of glycolysis. It is catalyzed by enolase into phosphoenolpyruvate (PEP), the penultimate step in the conversion of glucose to pyruvate.

2-Methylphenethylamine (2MPEA) is an organic compound with the chemical formula of C9H13N. 2MPEA is a human trace amine associated receptor 1 (TAAR1) agonist, a property which it shares with its monomethylated phenethylamine isomers, such as amphetamine (α-methylphenethylamine), β-methylphenethylamine, and N-methylphenethylamine (a trace amine). Very little data, even on toxicity, is available about its effects on humans other than that it activates the human TAAR1 receptor.

2-O-methyl-l-inositol

β-methylnaphthalene

2-acetyl-1-alkyl-sn-glycerol acetylhydrolase

2-Phenyl-1H-indole

2-Pentene

2-Phenyl-3,6-dimethylmorpholine is a drug with stimulant and anorectic effects, related to phenmetrazine. Based on what is known from other phenylmorpholines with similar structure, it likely acts as a serotonin reuptake inhibitor and may produce antidepressant-like effects.

2-Trifluoromethyl-4-(amino)-benzonitrile

2-Nitrophenyl-bD-galactopyranoside

2-alpha-D-glucosyl-D-glucose:phosphate beta-D-glucosyltransferase

2-alkenal reductase

Phenethyl bromide

2-Ray Ground Reflection Model

2-Methylfuran

2-Methyl-3-phenylpiperidine

2-Methyltetrahydrofuran-3-one

2-Piece handicap

o-Nitrotoluene, o-Methylnitrobenzene, 2-Methylnitrobenzene, ortho-Nitrotoluene

2-Octyne

2-Tolidine

1st Special Forces Airborne Regiment (Philippines)

2-Player Bullseye (The Price is Right pricing game)

1,3-dihydroxypropan-2-yl (Z)-octadec-9-enoate

MPK

2-Methylhexane

2-Quinolone

2-X

2-Ethenylpyridine

2-Propanone

Octan-2-yl 2-cyanoprop-2-enoate

sec-Caprylic alcohol

2-Piperidinone (2-piperidone or δ-valerolactam) is a chemical compound classified as a lactam. It is used as an intermediate in the preparation of other chemicals.

2-Methylbutan-2-ol

2-Hydroxynaphthalene; 2-Naphthalenol; beta-Naphthol; Naphth-2-ol

2-pentanone

2-Pyrrolidinone

2-Phenylhexane

2-V

2-Phospho-L-lactate guanylyltransferase

2-Methylbutyric acid

2-actionism

2-Tone

2-Player Auction (The Price is Right pricing game)

2-acetylpyridine

2-Piperidone

2-Methylpropan-2-ol

2-Propynyl alcohol

2-Naphthylamine

2-Star

2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose hydrolase

o-Nitrobenzoic acid

2-Methylhexane (C7H16, also known as isoheptane, ethylisobutylmethane) is an isomer of heptane. It is structurally a hexane molecule with a methyl group attached to its second carbon atom. It exists in most commercially available heptane merchandises as an impurity but is usually not considered as impurity in terms of reactions since it has very similar physical and chemical properties when compared to n-heptane (straight-chained heptane). Being an alkane, 2-methylhexane is insoluble in water, but is soluble in many organic solvents, such as alcohols and ether. However, 2-methylhexane is more commonly considered as a solvent itself. Therefore, even though it is present in many commercially available heptane products, it is not considered as a destructive impurity, as heptane is usually used as a solvent. Nevertheless, by concise processes of distillation and refining, it is possible to separate 2-methylhexane from n-heptane. Within a group of isomers, those with more branches tend to ignite more easily and combust more completely. Therefore, 2-methylhexane has a lower Autoignition temperature and flash point when compared to heptane. Theoretically 2-methylhexane also burns with a less sooty flame, emitting higher-frequency radiation; however, as heptane and 2-methylhexane differ by only one carbon atom, in terms of branching, both burn with a bright yellow flame when ignited. Compared to n-heptane, 2-methylhexane also has lower melting and boiling points. A lower density of liquid is found in 2-Methylhexane than heptane. On the NFPA 704 scale, 2-methylhexane is listed as a reactivity level-0 chemical, along with various other alkanes. In fact, most alkanes are unreactive except in extreme conditions, such as combustion or strong sunlight. At the presence of oxygen and flame, 2-methylhexane, like heptane, combusts mostly completely into water and carbon dioxide. With UV-light and mixed with halogens in solvents, usually bromine in 1,1,1-trichloroethane, a substitution reaction occurs.

2-Phenyl propylene

2-Z (album)

2-Propylheptan-1-ol

2-Nitrocinnamaldehyde

2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranose

In enzymology, a 2-acylglycerol-3-phosphate O-acyltransferase (EC 2.3.1.52) is an enzyme that catalyzes the chemical reaction acyl-CoA + 2-acyl-sn-glycerol 3-phosphate CoA + 1,2-diacyl-sn-glycerol 3-phosphate Thus, the two substrates of this enzyme are acyl-CoA and , whereas its two products are CoA and .

Pyrrolidin-2-one

2-Phenylethanol

2-Oxopent-4-enoic acid

2-Methylacetoacetyl-CoA is an intermediate in the metabolism of isoleucine.

2-Thiol-L-histidine-betaine

2-Methyltetrahydrofuran, 2-Methyl-THF

2-Methyl-3-pentanol

In enzymology, a 2-acylglycerol-3-phosphate O-acyltransferase (EC 2.3.1.52) is an enzyme that catalyzes the chemical reaction acyl-CoA + 2-acyl-sn-glycerol 3-phosphate CoA + 1,2-diacyl-sn-glycerol 3-phosphate Thus, the two substrates of this enzyme are acyl-CoA and , whereas its two products are CoA and . This enzyme belongs to the family of transferases, specifically those acyltransferases transferring groups other than aminoacyl groups. The systematic name of this enzyme class is acyl-CoA:2-acyl-sn-glycerol 3-phosphate O-acyltransferase. This enzyme is also called 2-acylglycerophosphate acyltransferase. This enzyme participates in glycerophospholipid metabolism.

2-Phenyl-3-aminobutane (also known as β-methylamphetamine) is a stimulant of the phenethylamine class that is closely related to its α-methyl analog Pentorex. It was first synthesized by the German scientists Felix Haffner and Fritz Sommer in 1939 as a stimulant with milder effects, shorter duration, lower toxicity and fewer side effects compared to previously known drugs such as amphetamine. 2-Phenyl-3-aminobutane is banned in some countries as a structural isomer of methamphetamine.

2-Propenoyl group

3,4-Dihydro-2(1H)-naphthalenone

Nitrobenzaldehyde

In enzymology, a 2-acetolactate mutase (EC 5.4.99.3) is an enzyme that catalyzes the chemical reaction 2-acetolactate 3-hydroxy-3-methyl-2-oxobutanoate Hence, this enzyme has one substrate, , and one product, . This enzyme belongs to the family of isomerases, specifically those intramolecular transferases transferring other groups. The systematic name of this enzyme class is 2-acetolactate methylmutase. Other names in common use include acetolactate mutase, and acetohydroxy acid isomerase. This enzyme participates in . It employs one cofactor, ascorbate.

2-Player Bullseye "I" (The Price is Right pricing game)

2-Methyl-5-hydroxytryptamine (2-Methylserotonin, 2-Methyl-5-HT) is a tryptamine derivative closely related to the neurotransmitter serotonin which acts as a moderately selective full agonist at the 5-HT3 receptor.

2-Nitrochlorobenzene is an organic compound with the formula ClC6H4NO2. It is one of three isomeric nitrochlorobenzenes. It is a yellow crystalline solid that is important as a precursor to other compounds due to its two functional groups.

2-Methylpyridine

2-Spirit

2-Methylpentane-2,4-diol

In enzymology, a 2-alkyn-1-ol dehydrogenase (EC 1.1.1.165) is an enzyme that catalyzes the chemical reaction 2-butyne-1,4-diol + NAD+ 4-hydroxy-2-butynal + NADH + H+ Thus, the two substrates of this enzyme are 2-butyne-1,4-diol and NAD+, whereas its 3 products are , NADH, and H+. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is 2-butyne-1,4-diol:NAD+ 1-oxidoreductase.

2- 7 Avenue White Plains Road Express

2-Methylisoborneol (MIB) is an organic chemical with a strong odor. It is a derivate of borneol. Its odor detection threshold is very low and it is one of the chemicals with major influence on the quality of drinking water. MIB is also a factor in cork taint in winemaking. Some algae, particularly blue-green algae (cyanobacteria) such as Anabaena, produce MIB together with other odorous chemicals such as geosmin. They give a musty or earthy odor that can be quite strong if an algal bloom is present. Subsequent death of the cyanobacteria will also release MIB that is trapped in the cells. These chemicals can be smelled at very low levels, in the parts-per-trillion range (ppt range), and are responsible for many "taste and odor" issues in drinking water treatment and distribution. Along with geosmin, the off flavors caused are issues in the seafood industry. This chemical is the major cause of "muddy" or "dirt" flavors in catfish and crawfish. Cyanobacteria can also produce chemical toxins that have been a problem in drinking water in some cases.

2-Pyrocatechuic acid

2-Nitrochlorobenzene

2-O

2-Nitrotoluene or ortho-nitrotoluene is an organic compound with the formula CH3C6H4NO2. It is pale yellow liquid that is a versatile intermediate in the production of various dyes.

2-Pentanone or methyl propyl ketone (MPK) is a ketone and solvent of minor importance. It is comparable to methyl ethyl ketone, but has a lower solvency and is more expensive. It occurs naturally in Nicotiana tabacum (Tobacco) and blue cheese as a metabolic product of Penicillium mold growth.

2-Phenylhexane is an aromatic hydrocarbon. It can be produced by a Friedel-Crafts alkylation between and benzene., or by the reaction of benzene and 1-hexene with various acid catalysts such as antimony pentafluoride, scandium(III) triflate, and phosphoric acid.

2-Tone Entertainment

2-Methylpentane, trivially known as isohexane, is a branched-chain alkane with the molecular formula C6H14. It is a structural isomer of hexane composed of a methyl group bonded to the second carbon atom in a pentane chain.

2- and 3-Part Inventions

2-Methylbutyryl-CoA dehydrogenase deficiency

2-Tone Entertainment is a British based independent record label and A&R consultancy company, who also specialise in Talent Management. The company was founded by Shaurav D'Silva in 2004. 2-Tone Entertainment have worked alongside 3 Beat Records & the Universal Music Group since 2011 successfully launching the careers of a number of artists including Sigma (group) and Fuse ODG . 2-Tone Entertainment represent a number of writers, producers and artists including Diztortion, Taya, Ts7 & Eyelar. They have also consulted for a number of urban entertainment and lifestyle brands such as SBTV and MOBO. On September 8, 2016, Warner Music announced the launch of new record label imprint in conjunction with 2-Tone Entertainment called 2TE Records. The label is set to launch in January 2017 and will be headed by 2-Tone founder Shaurav D'Silva.

2-PAM chloride

2-Phenylindole is an organic compound. It is the parent structure of a group of nonsteroidal selective estrogen receptor modulators (SERMs) that includes zindoxifene, bazedoxifene, and pipendoxifene, as well as the nonsteroidal estrogen D-15414 (the major metabolite of zindoxifene).

Pent-2-yne

The 2-Piece (二枚落ち nimai-ochi) handicap in shogi has both of White's major pieces (the rook and the bishop) removed. Thus, White is left with pawns, golds, silvers, knights, and lances. Black has the usual setup of twenty pieces. The 2-Piece handicap is an official handicap of the Japan Shogi Association.

Tweede afdeling, vliegtuiggroep vijf (second division, squadron five) or short 2-VLG-V was a squadron of the Royal Netherlands East Indies Army Air Force from the 1st of July 1941 to the 8th of March 1942.

2-acylglycerol O-acyltransferase

2-Y

2-VLG-V (ML-KNIL)

2-polyprenyl-6-hydroxyphenyl methylase

2-Methylphenethylamine

2-Methyl-6-(phenylethynyl)pyridine (MPEP) is a research drug which was one of the first compounds found to act as a selective antagonist for the metabotropic glutamate receptor subtype mGluR5. After being originally patented as a liquid crystal for LCDs, it was developed by the pharmaceutical company Novartis in the late 1990s. It was found to produce neuroprotective effects following acute brain injury in animal studies, although it was unclear whether these results were purely from mGluR5 blockade as it also acts as a weak NMDA antagonist, and as a positive allosteric modulator of another subtype mGlu4, and there is also evidence for a functional interaction between mGluR5 and NMDA receptors in the same populations of neurons. It was also shown to produce antidepressant and anxiolytic effects in animals, and to reduce the effects of morphine withdrawal, most likely due to direct interaction between mGluR5 and the μ-opioid receptor. The main significance of MPEP has been as a lead compound to develop more potent and selective mGluR5 antagonists such as MTEP, but research using MPEP itself continues, and recently it was shown to reduce self-administration of nicotine, cocaine, ketamine and heroin in animals, possibly through an MPEP-induced potentiation of the rewarding effect of the self-administered drug, and MPEP was also shown to possess weak reinforcing effects by itself.

2-Octanol (octan-2-ol, 2-OH) is a fatty alcohol. It is a secondary eight-carbon chiral compound. 2-Octanol is a colorless liquid that is poorly soluble in water but soluble in most organic solvents. It is used such as or as a raw material in various applications: flavors and fragrances, paints and coatings, inks, adhesives, home care, lubricants and fuels.2-Octanol can be a biobased alternative of 2-ethylhexanol and its derivates in numerous applications.

2-Methylhexane (C7H16, also known as isoheptane, ethylisobutylmethane) is an isomer of heptane. It is structurally a hexane molecule with a methyl group attached to its second carbon atom. It exists in most commercially available heptane merchandises as an impurity but is usually not considered as impurity in terms of reactions since it has very similar physical and chemical properties when compared to n-heptane (straight-chained heptane). Compared to n-heptane, 2-methylhexane also has lower melting and boiling points. A lower density of liquid is found in 2-Methylhexane than heptane.

2-Nitro-9H-fluorene

2-Methylheptane is a branched alkane isomeric to octane. Its structural formula is (CH3)2CH(CH2)4CH3.

2-acetamido-2-deoxy-D-glucose 6-sulfate sulfatase

2-Oxohistidine is a form of histidine damaged by reactive oxygen species. It can serve as a biological marker for assessing protein modifications from oxidative stress.

2-Naphthol

2-Methylaminoethanol

2-Octyl cyanoacrylate

2-Vinylpyridine is an organic compound with the formula CH2CHC5H4N. It is a derivative of pyridine with a vinyl group in the 2-position, next to the nitrogen. It is a colorless liquid, although samples are often brown. It is used industrially as a precursor to specialty polymers and as an intermediate in the chemical, pharmaceutical, dye, and photo industries.

2-Thioglycolic acid

2-U

2-Methylisoborneol (MIB) is an organic chemical with a strong odor. It is a derivate of borneol. Its odor detection threshold is very low and it is one of the chemicals with major influence on the quality of drinking water. MIB is also a factor in cork taint in winemaking.

2-Methyl-DMT

2-Phenylpyridine is an organic compound with the formula C6H5C5H4N. It is a colourless viscous liquid. The compound and related derivatives have attracted interest as precursors to highly fluorescent metal complexes of possible value as organic light emitting diodes (OLEDs). The compound is prepared by the reaction of phenyl lithium with pyridine: C6H5Li + C5H5N → C6H5-C5H4N + LiH The reaction of iridium trichloride with 2-phenylpyridine proceeds via cyclometallation to give the chloride-bridged complex: 4 C6H5-C5H4N + 2 IrCl3(H2O)3 → Ir2Cl2(C6H4-C5H4N)4 + 4 HCl This complex can be converted to the pictured tris(cyclometallated) derivative.

2H-Pyran-2-one

2-Phenyl-hexane

2-Naphthalenethiol

2-Chloronitrobenzene

In enzymology, a 2-alkenal reductase (EC 1.3.1.74) is an enzyme that catalyzes the chemical reaction n-alkanal + NAD(P)+ alk-2-enal + NAD(P)H + H+ The 3 substrates of this enzyme are n-alkanal, NAD+, and NADP+, whereas its 4 products are alk-2-enal, NADH, NADPH, and H+.

2-Pac

2-acylglycerophosphocholine

2-Pivalyl-1,3-indandione

2-QAM

2-alkyn-1-ol dehydrogenase

Biphenylol

2,3,4,5-tetramethoxyamphetamine

2-Methyltetrahydro-3-furanone

2-acetolactate mutase

2-NBDG

2-alarm fire

2-Methyloxolane

In enzymology, a 2-alkenal reductase (EC 1.3.1.74) is an enzyme that catalyzes the chemical reaction n-alkanal + NAD(P)+ alk-2-enal + NAD(P)H + H+ The 3 substrates of this enzyme are n-alkanal, NAD+, and NADP+, whereas its 4 products are alk-2-enal, NADH, NADPH, and H+. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-CH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is n-alkanal:NAD(P)+ 2-oxidoreductase. Other names in common use include NAD(P)H-dependent alkenal/one oxidoreductase, and NADPH:2-alkenal alpha,beta-hydrogenase.

In enzymology, a 2-acylglycerol O-acyltransferase (EC 2.3.1.22) is an enzyme that catalyzes the chemical reaction acyl-CoA + 2-acylglycerol CoA + diacylglycerol Thus, the two substrates of this enzyme are acyl-CoA and , whereas its two products are CoA and diacylglycerol. This enzyme belongs to the family of transferases, specifically those acyltransferases transferring groups other than aminoacyl groups. The systematic name of this enzyme class is acyl-CoA:2-acylglycerol O-acyltransferase. Other names in common use include acylglycerol palmitoyltransferase, monoglyceride acyltransferase, acyl coenzyme A-monoglyceride acyltransferase, and monoacylglycerol acyltransferase. This enzyme participates in .

2-N

2-Methylburtyryl-coenzyme A

2-Tetralinylamine

2-Quinolone is an organic compound related structurally to quinoline. It is the majority tautomer in equilibrium with 2-quinolinol. The compound can be classified as a cyclic amide, and as such is used as a isostere for peptides and other pharmaceutically-inspired targets. The isomer 4-quinolone is the parent of a large class of quinolone antibiotics. One example is .

2-acetylfuran

2-Rives

2-almost prime

2-Norbornyl cation

In enzymology, a 2-acylglycerophosphocholine O-acyltransferase (EC 2.3.1.62) is an enzyme that catalyzes the chemical reaction acyl-CoA + 2-acyl-sn-glycero-3-phosphocholine CoA + phosphatidylcholine Thus, the two substrates of this enzyme are acyl-CoA and , whereas its two products are CoA and phosphatidylcholine.

2-Ten FM

2-Methylbutane

2-Methylidenebutanedioic acid

2-Methylindole

Octan-2-ol

2-Pyranone

2-Methyl-5-HT

Naphthalen-2-ol

2,3,4,6-Tetrahydroxybenzocyclohepten-5-one

Orthophenyl phenol
Orthoxenol

2-Phenylpyridine

2-alpha-D-glucosyl-D-glucose

2-Propylheptanol

2-Tone Entertainment is a British based independent record label and A&R consultancy company, who also specialise in Talent Management. The company was founded by Shaurav D'Silva in 2004. 2-Tone Entertainment have worked alongside 3 Beat Records & the Universal Music Group since 2011 successfully launching the careers of a number of artists including Sigma (group) and Fuse ODG .

2-Pyrroline

2-Phenethylamine

2-Z

Naphthalen-2-amine

2-T

2-SAT

2-Pentanone

1st of January

2-Pyrimidinyl-1-piperazine

2-Methylfuran is a flammable, water-insoluble liquid with a chocolate odor, found naturally in Myrtle and Dutch Lavenderused as a FEMA GRAS flavoring substance, with the potential for use in alternative fuels.

2-Octyne, also known as methylpentylethin and oct-2-yne, is a type of alkyne with a triple bond at its second carbon (the '2-' indicates the location of the triple bond in the chain). Its formula is C8H14. Its density at 25 °C and otherwise stable conditions is 0.759 g/ml. The boiling point is 137 °C. The average molar mass is 110.20 g/mol.

2-Aminoheptane

2-Pyrazinecarboxylic acid

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine

2-Azabiphenyl

2-Methylphenylpiperazine

2-Propanol

2-Nitrobenzaldehyde

2-Oxohistidine

2-Propynoic acid

2-Methylpentan-3-ol

2-TOM

2-acetyl-6-hydroxyneomycin C deacetylase

2-Propylamine

In organic chemistry, the term 2-norbornyl cation (or 2-bicyclo[2.2.1]heptyl cation) describes one of the three carbocations formed from derivatives of norbornane. Though 1-norbornyl and 7-norbornyl cations have been studied, the most extensive studies and vigorous debates have been centered on the exact structure of the 2-norbornyl cation. The 2-norbornyl cation has been formed from a variety of norbornane derivatives and reagents. First reports of its formation and reactivity published by Saul Winstein sparked controversy over the nature of its bonding, as he invoked a three-center two-electron bond to explain the stereoselectivity of the resulting product. Herbert C. Brown challenged this assertion on the grounds that classical resonance structures could explain the stereospecificity without needing to adapt a new perspective of bonding. Evidence of the non-classical nature of the 2-norbornyl cation grew over the course of several decades, mainly through spectroscopic data gathered using methods such as nuclear magnetic resonance (NMR). Crystallographic confirmation of its non-classical nature did not come until 2013. The nature of bonding in the 2-norbornyl cation incorporated many new ideas into the field’s understanding of chemical bonds. Similarities can be seen between this cation and others, such as boranes.

2-Player Bullseye I (The Price is Right pricing game)

2-Phenylethylbromide

2-Pyrone

2-Pyridone (data page)

2-Methylalanine

2-S-glutathionyl caftaric acid

(E)-3-(2-Nitrophenyl)prop-2-enal

2-Person Bobsled

2-Methylacetoacetyl-CoA

2-Player Bullseye (game show)

2-Phenylisopropylamine

2-acylglycero-3-phosphocholine

2-Methylpentane

2-a

2-(o-Tolyl)ethan-1-amine

2-Nitrobenzaldehyde is an organic aromatic compound containing a nitro group ortho to formyl. 2-Nitrobenzaldehyde once was produced as an intermediate in the synthesis of the popular dye Indigo.

2-Methyl-6-(phenylethynyl)pyridine (MPEP) is a research drug which was one of the first compounds found to act as a selective antagonist for the metabotropic glutamate receptor subtype mGluR5. After being originally patented as a liquid crystal for LCDs, it was developed by the pharmaceutical company Novartis in the late 1990s. It was found to produce neuroprotective effects following acute brain injury in animal studies, although it was unclear whether these results were purely from mGluR5 blockade as it also acts as a weak NMDA antagonist, and as a positive allosteric modulator of another subtype mGlu4, and there is also evidence for a functional interaction between mGluR5 and NMDA receptors in the same populations of neurons. It was also shown to produce antidepressant and anxiolytic ef

2-Methylnaphthalene

In organic chemistry, the term 2-norbornyl cation (or 2-bicyclo[2.2.1]heptyl cation) describes one of the three carbocations formed from derivatives of norbornane. Though 1-norbornyl and 7-norbornyl cations have been studied, the most extensive studies and vigorous debates have been centered on the exact structure of the 2-norbornyl cation. The nature of bonding in the 2-norbornyl cation incorporated many new ideas into the field’s understanding of chemical bonds. Similarities can be seen between this cation and others, such as boranes.

2-Methyl-butan-1-ol

2-Naphthylamine is one of two isomeric aminonaphthalenes, compounds with the formula C10H7NH2. It is a colorless solid, but samples take on a reddish color in air because of oxidation. It was formerly used to make azo dyes, but it is a known carcinogen and has largely been replaced by less toxic compounds.

2-Methyl-5-(1-methylethyl)-phenol

2-OCA

2-Oxoglutarate

2-Methylaziridine

(Naphthalen-2-yl)amine

2-Oxachloromadinone

2-Methylisoborneol

2-acetamido-2-deoxy-D-galactose

2-MeIm

Hexan-2-ylbenzene

2-TOET

2-Methylpyrazine

2,3,4,7,8-Pentachlorodibenzofuran

2-Nitrobenzenamine

2-Propenenitrile

2-TEN FM

2-Methylpropenoic acid

2-Oxohexamethyleneimine

2-Methylnaphthalene is a polycyclic aromatic hydrocarbon (PAH). On February 22, 2014, NASA announced a greatly upgraded database for detecting and monitoring PAHs, including 2-methylnaphthalene, in the universe. According to NASA scientists, over 20% of the carbon in the universe may be associated with PAHs, possible starting materials for the formation of life. PAHs seem to have been formed shortly after the Big Bang, are abundant in the universe, and are associated with new stars and exoplanets. Several enzymes biodegrade 2-methyhlnaphthalene in anaerobic conditions.

2-acetylcocaine

2-OG

2-Methyl-3-pentanol (IUPAC name: 2-methylpentan-3-ol) is an organic chemical compound. It is used as a fuel.

2-Phosphoglyceric acid

1-Methyl-1-heptanol

3-(2-Oxo-2H-imidazol-4-yl)alanine

"2-Way" is the first single from Lil' Romeo's second studio album Game Time. The track features additional vocals from his dad Master P and Silkk The Shocker. It is an almost-complete cover of "It Takes Two" by Rob Base and DJ E-Z Rock, with slight lyrical alterations to the original (i.e. references in Base's own lyrics to himself) and additional samples. The song was played at the ending credits of Hey Arnold!: The Movie.

2-Nonanol is a simple alcohol. It has the odor of cucumber, and has been identified in oysters. It is used by several insects as pheromones. It is commercially available.

1st Special Forces Command (Airborne)

ortho-Nitrobenzaldehyde

2-Step

2-Monoolein

2-Methylaniline

2-Succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid synthase

Capryl alcohol

2-Nonenal

2-Nitrofluorene is a by-product of combustion and is a nitrated polycyclic aromatic hydrocarbon (fluorene). 2-Nitrofluorene is listed as an IARC Group 2B carcinogen, indicating it is possibly carcinogenic to humans.

2-Toluidine

2-acetamidofluorene:NAD(P)+ oxidoreductase

2-Methylbenzeneethanamine

2-Methylene glutaronitrile is a dimerization product of acrylonitrile and a starting material for di- and triamines, for the biocide 2-bromo-2-(bromomethyl)pentanedinitrile and for heterocycles, such as 3-cyanopyridine.

2-Phenyl-3-aminobutane

2-acetoxypropane

2-Methylbutyryl-CoA

2-Methyl-4-chlorophenoxyacetic acid

2-Oxiranecarboxylic acid

2-Methyl-2-bornanol

2-acetylaminofluorene

2-Undecanone,1

1,2,7,7-tetramethylbicyclo[2.2.1]heptan-2-ol

2-Phenyl-3,6-dimethylmorpholine

2VP

2-Methylcyclopentadienyl manganese tricarbonyl

2-Tetralone is an organic chemical compound with the molecular formula C10H10O. This colourless oil is an intermediate in organic synthesis. It is a ketone derivative of tetralin, a hydrogenated derivative of naphthalene. A related compound is 1-tetralone. 2-Tetralone is prepared by reductive cleavage of 2-naphthyl ethers.

2-adic order

2-Methylbutan-1-ol

2-Oxoquazepam (Sch 15725) is a benzodiazepine derivative and one of the major active metabolites of quazepam (Doral).

2-acetyloxybenzoic acid

2-S

2-Nitrocinnamaldehyde, ortho-nitrocinnamaldehyde or o-nitrocinnamaldehyde is an organic aromatic compound containing a nitro group ortho- to the 1-position of cinnamaldehyde.

2-Propenyl propyl disulfide

2-Propenamide

2,4-dicyano-1-butene

2-alpha-mannosyl-oligosaccharide alpha-D-mannohydrolase

2-NBDG is a fluorescent tracer used for monitoring glucose uptake into living cells; it consists of a glucosamine molecule substituted with a 7-nitrobenzofurazan fluorophore at its amine group. It is widely referred to a fluorescent derivative of glucose, and it is used in cell biology to visualize uptake of glucose by cells. Cells that have taken up the compound fluoresce green. Like glucose, 2-NBDG is transported according to Michaelis-Menten kinetics. However, transport of 2-NBDG has a lower Vmax (maximum rate), and thus the rate of transport is generally slower than glucose.

2-Player Bullseye

2-Phenylpyridine is an organic compound with the formula C6H5C5H4N. It is a colourless viscous liquid. The compound and related derivatives have attracted interest as precursors to highly fluorescent metal complexes of possible value as organic light emitting diodes (OLEDs). The compound is prepared by the reaction of phenyl lithium with pyridine: C6H5Li + C5H5N → C6H5-C5H4N + LiH The reaction of iridium trichloride with 2-phenylpyridine proceeds via cyclometallation to give the chloride-bridged complex: 4 C6H5-C5H4N + 2 IrCl3(H2O)3 → Ir2Cl2(C6H4-C5H4N)4 + 4 HCl

2-Methylpropene

2-Methyl-3-phenylpiperidine is a psychostimulant.

2-PAM

2-Oxobutyrate

2-acetylpyrazine

2-Pyrimidinylpiperazine

2-Octanol

2-Trifluoromethyl-4-amino-benzonitrile

2-alpha-methyl-3-hydroxybutyricacidemia

2-O-(6-phospho-mannosyl)-D-glycerate hydrolase, alpha-mannosidase

2-OH-E1

2-Tetralone

2-Hydroxybiphenyl

Methylketol or 2-methylindole is a mildly toxic and slightly flammable organic compound which occurs as a white solid which turns brown over time. It has chemical formulaC9H9N. Methylketol is used as an intermediate for synthesizing dyes, pigments, optical brighteners, and pharmaceuticals.

2-acylglycerol-3-phosphate O-acyltransferase

2-Way (Lil' Romeo song)

2-N,6-O-disulfo-D-glucosamine 6-sulfohydrolase

2-Trifluoromethyl-4-(amino)benzonitrile

2-OHE1

2-Phenyl propane

2-Tone records

2-Nitrofluorene

2-Naphthalenethiol is an organosulfur compound with the formula C10H7SH. It is a white solid. It is one of two monothiols of naphthalene, the other being 1-naphthalenethiol. 2-Naphthalenethiol is prepared from 2-naphthol by the Newman–Kwart rearrangement using the thiocarbamate. It undergoes lithiation at the 3-position. It can be used as a flavouring agent.

In enzymology, a 2-acylglycerophosphocholine O-acyltransferase (EC 2.3.1.62) is an enzyme that catalyzes the chemical reaction acyl-CoA + 2-acyl-sn-glycero-3-phosphocholine CoA + phosphatidylcholine Thus, the two substrates of this enzyme are acyl-CoA and , whereas its two products are CoA and phosphatidylcholine. This enzyme belongs to the family of transferases, specifically those acyltransferases transferring groups other than aminoacyl groups. The systematic name of this enzyme class is acyl-CoA:2-acyl-sn-glycero-3-phosphocholine O-acyltransferase. Other names in common use include 2-acylglycerol-3-phosphorylcholine acyltransferase, and 2-acylglycerophosphocholine acyltransferase. This enzyme participates in glycerophospholipid metabolism.

2-acetyl-5-methylfuran

2-Pyridinethiol 1-oxide

2-Phenylethylhydrazine

2-Keto-4-pentenoic acid

2-Piperidinone

2-R

2-Methyltetrahydrofuran is an organic compound with the molecular formula CH3C4H7O. It is a highly flammable mobile liquid. It is mainly used as a replacement for THF in specialized applications for its better performance, such as to obtain higher reaction temperatures, or easier separations (as, unlike THF, it is not miscible with water). It is derived from sugars via furfural and is occasionally touted as a biofuel.

2-Phenylindole

2-Tone Records

o-Xenol

2-Nitrobenzoic acid is an organic compound with the formula C6H4(NO2)CO2H. It is prepared by oxidation of 2-nitrotoluene with nitric acid.

2-Pyridylethylamine

β-Naphthylamine

δ-Valerolactam; Piperidin-2-one; 2-Piperidone

2-Methylpentan-2-ol

Ethylmethylacetylene, 1-Ethyl-2-methylacetylene propyl acetylene

Naphthalene-2-thiol

2,5-dimethoxy-4-n-propylthiophenethylamine

2-O-alpha-L-Rhamnosyl-D-glucose

2- and 4-Quinolones

2-Methylpropanoyl chloride

β-Tetralone; 2-Tetralone

2-Pyrone (α-pyrone or pyran-2-one) is an unsaturated cyclic chemical compound with the molecular formula C5H4O2. It is isomeric with 4-pyrone. 2-Pyrone is used in organic synthesis as a building block for more complex chemical structures because it may participate in a variety of cycloaddition reactions to form bicyclic lactones. For example, it readily undergoes Diels-Alder reactions with alkynes producing, upon loss of carbon dioxide, substituted benzenes. The Gogte Synthesis (1938) is a method for the alkylation of certain pyrones with acid chlorides.

2-O-(6-phospho-alpha-D-mannosyl)-D-glycerate acylhydrolase

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2-Pentyne, an organic compound, is an internal alkyne. It is an isomer of 1-pentyne, a terminal alkyne.

2-Oxopent-4-enoic acid (2-oxopent-4-enoate) is formed by the dehydration of 4-hydroxy-2-oxopentanoate by 2-oxopent-4-enoate hydratase or by the hydrolysis of 2-hydroxymuconate semialdehyde by 2-hydroxymuconate-semialdehyde hydrolase.

1st of July

2-(2-Methylphenyl)ethan-1-amine

Ethyl isopropyl carbinol

2-acetolactate methylmutase

2-(2-Methylphenyl)ethanamine

1-Chloro-2-nitrobenzene

2-Phenylphenol, or o-phenylphenol, is an organic compound. In terms of structure, it is one of the monohydroxylated isomers of biphenyl. It is a white solid. It is a biocide used as a preservative with E number E231 and under the trade names Dowicide, Torsite, Fungal, Preventol, Nipacide and many others.

2-Phenoxyethanol

2-Methylacrylic acid

2-Nitrotoluene

2-Rivières

2-O-alpha-L-Rhamnopyranosyl-D-glucopyranose

In enzymology, SEPHCHC synthase (EC EC 2.2.1.9), encoded by menD gene in E. coli, is an enzyme that catalyzes the second step of menaquinone (vitamin K2) biosynthesis. The two substrates of this enzyme are 2-oxoglutarate and . The products of this enzyme are 5-enolpyruvoyl-6-hydroxy-2-succinyl-cyclohex-3-ene-1-carboxylate and CO2. It belongs to the transferase family.

methyl propyl ketone

2-Picoline

2-Phenylethylamine

2-Phospho-L-lactate guanylyltransferase (EC 2.7.7.68, CofC, MJ0887) is an enzyme with systematic name GTP:2-phospho-L-lactate guanylyltransferase. This enzyme catalyses the following chemical reaction (2S)-2-phospholactate + GTP (2S)-lactyl-2-diphospho-5'-guanosine + diphosphate This enzyme is involved in the biosynthesis of coenzyme F420.

2-Phenylisopropylhydrazine

2-Pyridylethylamine is a histamine agonist which is selective for the H1 subtype.

2-NBDG is a fluorescent tracer used for monitoring glucose uptake into living cells; it consists of a glucosamine molecule substituted with a 7-nitrobenzofurazan fluorophore at its amine group. It is widely referred to a fluorescent derivative of glucose, and it is used in cell biology to visualize uptake of glucose by cells. Cells that have taken up the compound fluoresce green. 2-NBDG is similar to radiolabeled glucose in that both can be used to detect glucose transport. Unlike radiolabeled glucose, 2-NBDG is compatible with fluorescence techniques such as a fluorescent microscopy, flow cytometry, and fluorimetry The compound is taken up by a variety of mammalian, plant, and microbial cells In mammalian cells, one transporter for 2-NBDG is GLUT2. In bacterial cells, the predominant transporter is the mannose phosphotransferase system. Cells that lack these or other compatible transporters do not take up 2-NBDG. Like glucose, 2-NBDG is transported according to Michaelis-Menten kinetics. However, transport of 2-NBDG has a lower Vmax (maximum rate), and thus the rate of transport is generally slower than glucose. Once taken up, the compound is metabolized to a non-fluorescent derivative, as shown in Escherichia coli. The identity and further metabolism of this non-fluorescent derivative has not been established.

2-OH-NPA is a drug used in scientific research which acts as a potent and selective agonist for the dopamine D2 receptor.

2-Ocean Navy act

2-Oxoquazepam

2-Methylbutyryl-coenzyme A

2-Nitrophenol

Amylmethylacetylene; Methylpentylacetylene

D-Glucose, 2-deoxy-2-((7-nitro-2,1,3-benzoxadiazol-4-yl)amino)-

Pyran-2-one

The 1st Special Forces Command (Airborne) is a division-level special operation forces command within the US Army Special Operations Command. The command was established on 30 September 2014, grouping together the Army Special Forces (a.k.a. the Green Berets), Psychological Operations (or PSYOP), Civil Affairs, and support troops into a single organization operating out of its new headquarters building at Fort Bragg, NC.

2-Oleoylglycerol (2OG) is a monoacylglycerol that is found in biologic tissues. Its synthesis is derived from diacylglycerol precursors. It is metabolized to oleic acid and glycerol primarily by the enzyme monoacylglycerol lipase (MAGL). In 2011, 2OG was found to be an endogenous ligand to GPR119. 2OG has been shown to increase glucagon-like peptide-1 (GLP-1) and gastric inhibitory polypeptide (GIP) levels following administration to the small intestine.

2-Biphenylol

2-Phenylquinoline-4-carboxylic acid

2-NBD Glucose

2-Methylnitrobenzene

2PG

Methylhexylcarbinol
2-Octyl alcohol

2-Rivieres

2-SAP

2-Propen-1-ol

2-alpha-L-fucopyranosyl-beta-D-galactoside fucohydrolase

2-Phenylcyclopentylamine

Isohexane

2-Methylethyleneimine

2-Up

2-Methyleneglutaronitrile

2-acetamidofluorene

2-O-(6-phospho-mannosyl)-D-glycerate hydrolase

nonan-2-ol

2-Methylamphetamine

2-acetyl-1-pyrroline
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2-Methyltetrahydrofuran

2-Q

2-Methylpropane

2-Methyl-5-hydroxytryptamine

2-Octyl 2-cyanoacrylate; 1-Methylheptyl cyanoacrylate

2-S-adenosyl-L-homocysteine

2-Polyprenyl-6-hydroxyphenyl methylase

2-Phenylpropylamine

2-Phosphoglycerate

3-hydroxy-2-phosphonooxypropanoic acid

o-Phenylphenol

2-Step Garage

2-Nonanol

2-Propenoyl

2-adic integers

2-Methyl-1H-imidazole

2-OH-NPA

2-Methylbenzoic acid

2-S-glutathionylcaftaric acid

2-Trifluoromethyl-4-aminobenzonitrile

2-Oxetanone

2-Methylimidazole

2-Bromoethylbenzene

2-acylglycerophosphocholine O-acyltransferase