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179051

Sigma-Aldrich

trans-2-Phenyl-1-cyclohexanol

99%

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About This Item

Linear Formula:
C6H5C6H10OH
CAS Number:
2362-61-0
Molecular Weight:
176.25
Beilstein:
3198908
EC Number:
219-111-2
MDL number:
MFCD00003865
UNSPSC Code:
12352100
PubChem Substance ID:
24850795
NACRES:
NA.22

Assay

99%

form

solid

bp

152-155 °C/16 mmHg (lit.)

mp

53-55 °C (lit.)

SMILES string

O[C@@H]1CCCC[C@H]1c2ccccc2

InChI

1S/C12H16O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-3,6-7,11-13H,4-5,8-9H2/t11-,12+/m0/s1

InChI key

AAIBYZBZXNWTPP-NWDGAFQWSA-N

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General description

The enantioselective resolution of trans-2-phenyl-1-cyclohexanol by Candida rugosa lipase was studied.

Application

trans-2-Phenyl-1-cyclohexanol was used in the synthesis of chiral compounds with high purity.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Kinetic resolution of chiral alcohols in bifunctional membrane exhibiting enzyme activity and enantioselective permeation.
Journal of Molecular Catalysis. B, Enzymatic, 24, 17-26 (2003)
A Sánchez et al.
Journal of biotechnology, 84(1), 1-12 (2000-10-18)
Enantioselective resolution of trans-2-phenyl-1-cyclohexanol (TPCH) by a Candida rugosa lipase, obtained by fermentation in the laboratory, and immobilised on EP100 polypropylene powder has been carried out using isooctane as solvent and propionic acid as esterifying agent. The study have included

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