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Merck
CN

179051

反-2-苯基-1-环己醇

99%

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线性分子式:
C6H5C6H10OH
化学文摘社编号:
分子量:
176.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-111-2
Beilstein/REAXYS Number:
3198908
MDL number:
Assay:
99%
Form:
solid
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InChI key

AAIBYZBZXNWTPP-NWDGAFQWSA-N

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

SMILES string

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

assay

99%

form

solid

bp

152-155 °C/16 mmHg (lit.)

mp

53-55 °C (lit.)

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.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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分析证书(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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