153087
2-Methylcyclohexanol, mixture of cis and trans
99%
Synonym(s):
Hexahydro-o-cresol
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About This Item
Linear Formula:
CH3C6H10OH
CAS Number:
Molecular Weight:
114.19
Beilstein/REAXYS Number:
1847535
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
99%
form
liquid
refractive index
n20/D 1.462 (lit.)
bp
163-166 °C (lit.)
density
0.93 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
CC1CCCCC1O
InChI
1S/C7H14O/c1-6-4-2-3-5-7(6)8/h6-8H,2-5H2,1H3
InChI key
NDVWOBYBJYUSMF-UHFFFAOYSA-N
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Application
2-Methylcyclohexanol was used to study the effect of organic solvents on epoxide hydrolase.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk_germany
WGK 1
flash_point_f
138.2 °F - closed cup
flash_point_c
59 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Jeanette Lotter et al.
Biotechnology letters, 26(15), 1191-1195 (2004-08-04)
Epoxides are often highly hydrophobic substrates and the presence of an organic co-solvent within an aqueous bioreactor is in such cases indicated. The effect of 40 water-miscible and -immiscible organic solvents on epoxide hydrolase activity in whole-cells of the yeast
Halis T Balaydın et al.
Bioorganic & medicinal chemistry letters, 22(3), 1352-1357 (2012-01-11)
The Naturally occurring novel cyclohexanonyl bromophenol 2(R)-2-(2,3,6-tribromo-4,5-dihydroxybenzyl)cyclohexanone (4) was synthesized as a racemic compound. Cyclohexylphenyl methane derivatives (10-17) with Br, OMe, CO, and OH were also obtained. Inhibition of four human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes I, II, IV
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