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153087

2-Methylcyclohexanol, mixture of cis and trans

Name: 2-Methylcyclohexanol, mixture of <I>cis</I> and <I>trans</I>
Brand: ALDRICH

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

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24849284

EC Number:

209-512-0

Beilstein/REAXYS Number:

1847535

MDL number:

MFCD00001443

Assay:

99%

Form:

liquid

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Properties

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

Description

Application

2-Methylcyclohexanol was used to study the effect of organic solvents on epoxide hydrolase.

pictograms

GHS02,GHS07

signalword

Warning

hcodes

H226,H302

pcodes

P210 - P233 - P240 - P241 - P242 - P301 + P312

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

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

Regulatory Information

危险化学品

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Correlation between the physicochemical properties of organic solvents and their biocompatibility toward epoxide hydrolase activity in whole-cells of a yeast, Rhodotorula sp.

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

Synthesis and carbonic anhydrase inhibitory properties of novel cyclohexanonyl bromophenol derivatives.

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

Global Trade Item Number

SKU	GTIN
661147-500MG	04061832250649
153087-1L	04061837014109
153087-250ML	04061838740663