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153087

Sigma-Aldrich

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:
583-59-5
Molecular Weight:
114.19
Beilstein:
1847535
EC Number:
209-512-0
MDL number:
MFCD00001443
UNSPSC Code:
12352100
PubChem Substance ID:
24849284
NACRES:
NA.22

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.)

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.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H302

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

138.2 °F - closed cup

Flash Point(C)

59 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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