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P24055

Sigma-Aldrich

1-Phenyl-1,2-ethanediol

97%

Sinónimos:

(±)-1-Phenyl-1,2-ethanediol, (±)-Phenylethylene glycol

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About This Item

Fórmula lineal:
C6H5CH(OH)CH2OH
Número de CAS:
93-56-1
Peso molecular:
138.16
Beilstein/REAXYS Number:
1306723
EC Number:
202-258-1
MDL number:
MFCD00003546
UNSPSC Code:
12352100
PubChem Substance ID:
24898323
NACRES:
NA.22

assay

97%

form

solid

bp

272-274 °C/760 mmHg (lit.)

mp

66-68 °C (lit.)

SMILES string

OCC(O)c1ccccc1

InChI

1S/C8H10O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8-10H,6H2

InChI key

PWMWNFMRSKOCEY-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Ashwini C Mathpati et al.
Journal of biotechnology, 262, 1-10 (2017-09-30)
Kinetic resolution of rac-1,2-diols using the biocatalyst Burkholderia cepacia lipase (BCL) immobilized on a biodegradable binary blend support of hydroxypropyl methyl cellulose(HPMC)/polyvinyl alcohol (PVA) has been investigated. The immobilization technique improved enzyme activity significantly and it has excellent recyclability with
Li Cao et al.
Biotechnology and bioengineering, 94(3), 522-529 (2006-02-25)
Soluble epoxide hydrolase (EH) from the potato Solanum tuberosum and an evolved EH of the bacterium Agrobacterium radiobacter AD1, EchA-I219F, were purified for the enantioconvergent hydrolysis of racemic styrene oxide into the single product (R)-1-phenyl-1,2-ethanediol, which is an important intermediate
Cesar Mateo et al.
Analytical biochemistry, 314(1), 135-141 (2003-03-14)
In this paper we report the development of a novel and simple spectrophotometric assay which allows one to achieve the continuous, rapid, sensitive, and accurate determination of an epoxide hydrolase activity. This assay is based on the elaboration of a
O Spiegelstein et al.
Pharmaceutical research, 17(2), 216-221 (2000-04-06)
The purpose of this study was to evaluate the in vitro inhibitory potency of various amide analogues and derivatives of valproic acid toward human microsomal epoxide hydrolase (mEH). mEH inhibition was evaluated in human liver microsomes with 25 microM (S)-(+)-styrene
Yao Nie et al.
Organic & biomolecular chemistry, 9(11), 4070-4078 (2011-04-21)
The application of biocatalysis to the synthesis of chiral molecules is one of the greenest technologies for the replacement of chemical routes due to its environmentally benign reaction conditions and unparalleled chemo-, regio- and stereoselectivities. We have been interested in
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