28945
环己烷羧酸
purum, ≥97.0% (GC)
别名:
六氢苯甲酸
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线性分子式:
C6H11CO2H
化学文摘社编号:
分子量:
128.17
EC Number:
202-711-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
970529
MDL number:
grade
purum
assay
≥97.0% (GC)
refractive index
n20/D 1.461 (lit.)
bp
232-233 °C (lit.)
mp
29-31 °C (lit.)
density
1.033 g/mL at 25 °C (lit.)
SMILES string
OC(=O)C1CCCCC1
InChI
1S/C7H12O2/c8-7(9)6-4-2-1-3-5-6/h6H,1-5H2,(H,8,9)
InChI key
NZNMSOFKMUBTKW-UHFFFAOYSA-N
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT RE 2
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
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Janice C Paslawski et al.
Biodegradation, 20(1), 125-133 (2008-07-18)
Naphthenic acids are a complex mixture of organic compounds which naturally occur in crude oil. Low molecular weight components of the naphthenic acids are known to be toxic in aquatic environments and there is a need to better understand the
M J Liu et al.
Drug metabolism and disposition: the biological fate of chemicals, 20(6), 810-815 (1992-11-01)
The pharmacokinetics of valproic acid (VPA) and its structural analogs cyclohexanecarboxylic acid (CCA) and 1-methyl-1-cyclohexanecarboxylic acid (MCCA) were examined in bile-exteriorized rats. A 0.52 mmol/kg dose (equivalent to 75 mg/kg VPA) of test compound (N = 4 rats per compound)
Housna Mouttaki et al.
Applied and environmental microbiology, 75(4), 998-1004 (2008-12-31)
Transformations of 2-hydroxybenzoate and fluorobenzoate isomers were investigated in the strictly anaerobic Syntrophus aciditrophicus to gain insight into the initial steps of the metabolism of aromatic acids. 2-Hydroxybenzoate was metabolized to methane and acetate by S. aciditrophicus and Methanospirillum hungatei
S M Patton et al.
Biochemistry, 39(25), 7595-7604 (2000-06-20)
The side chain of the antifungal polyketide ansatrienin A produced by Streptomyces collinus contains a cyclohexanecarboxylic acid (CHC) derived moiety. This CHC in the coenzyme A activated form (CHC-CoA) is derived from shikimic acid via a pathway in which the
P Wang et al.
Journal of bacteriology, 178(23), 6873-6881 (1996-12-01)
We report the cloning of the gene encoding the 1-cyclohexenylcarbonyl coenzyme A reductase (ChcA) of Streptomyces collinus, an enzyme putatively involved in the final reduction step in the formation of the cyclohexyl moiety of ansatrienin from shikimic acid. The cloned
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