Synthetase, Acetylcoenzyme A

Suppliers

Names

[ CAS No. ]:
9012-31-1

[ Name ]:
Synthetase, Acetylcoenzyme A

[Synonym ]:
N-Acetyl-3,5-dinitro-L-tyrosine
WNR BQ CNW E1YVQMV1 &&L or S Form
L-Tyrosine, N-acetyl-3,5-dinitro-

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
583.2±50.0 °C at 760 mmHg

[ Molecular Formula ]:
C11H11N3O8

[ Molecular Weight ]:
313.220

[ Flash Point ]:
306.5±30.1 °C

[ Exact Mass ]:
313.054626

[ PSA ]:
181.76000

[ LogP ]:
0.43

[ Vapour Pressure ]:
0.0±1.7 mmHg at 25°C

[ Index of Refraction ]:
1.636

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

Articles

Incomplete Wood-Ljungdahl pathway facilitates one-carbon metabolism in organohalide-respiring Dehalococcoides mccartyi.

Proc. Natl. Acad. Sci. U. S. A. 111(17) , 6419-24, (2014)

The acetyl-CoA "Wood-Ljungdahl" pathway couples the folate-mediated one-carbon (C1) metabolism to either CO2 reduction or acetate oxidation via acetyl-CoA. This pathway is distributed in diverse anaer...

The genome sequence of Propionibacterium acidipropionici provides insights into its biotechnological and industrial potential.

BMC Genomics 13 , 562, (2012)

Synthetic biology allows the development of new biochemical pathways for the production of chemicals from renewable sources. One major challenge is the identification of suitable microorganisms to hol...

Purification and characterization of the acetyl-CoA synthetase from Mycobacterium tuberculosis.

Acta Biochim. Biophys. Sin. (Shanghai) 43(11) , 891-9, (2011)

Acetyl-CoA (AcCoA) synthetase (Acs) catalyzes the conversion of acetate into AcCoA, which is involved in many catabolic and anabolic pathways. Although this enzyme has been studied for many years in m...


More Articles

Related Compounds

  • Acetyl-CoA
  • Acyl coenzyme A synthetase
  • 2-Pyridineethanol, a-ethyl-a-(4-methoxyphenyl)-b-phenyl-, (aS,bS)-
  • Benzeneacetic acid, a-ethoxy-a-phenyl-, 2-(dimethylamino)ethylester, hydrochloride (9CI)
  • Avoparcin α
  • 1H-Cyclopropa[a]naphthalene
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide
  • N-[3-(Aminooxy)propyl]-N-butyl-1-butanamine