310298
(R)-(+)-Styrene oxide
98%
Synonym(s):
(R)-(+)-Phenyloxirane, (R)-Phenylethylene oxide
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About This Item
Empirical Formula (Hill Notation):
C8H8O
CAS Number:
Molecular Weight:
120.15
PubChem Substance ID:
UNSPSC Code:
12352005
Beilstein/REAXYS Number:
1984
MDL number:
assay
98%
optical activity
[α]18/D +33°, neat
optical purity
ee: 95% (HPLC)
autoignition temp.
928 °F
expl. lim.
~22 %
refractive index
n20/D 1.534 (lit.)
bp
89-90 °C/23 mmHg (lit.)
density
1.051 g/mL at 25 °C (lit.)
SMILES string
C1O[C@@H]1c2ccccc2
InChI
1S/C8H8O/c1-2-4-7(5-3-1)8-6-9-8/h1-5,8H,6H2/t8-/m0/s1
InChI key
AWMVMTVKBNGEAK-QMMMGPOBSA-N
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Daniel Kuhn et al.
Journal of industrial microbiology & biotechnology, 39(8), 1125-1133 (2012-04-25)
Selection of the ideal microbe is crucial for whole-cell biotransformations, especially if the target reaction intensively interacts with host cell functions. Asymmetric styrene epoxidation is an example of a reaction which is strongly dependent on the host cell owing to
Michael Kotik et al.
Journal of biotechnology, 156(1), 1-10 (2011-08-23)
We performed a laboratory evolution study with the epoxide hydrolase from Aspergillus niger M200. This enzyme exhibits no enantioconvergence with the substrates styrene oxide or para-chlorostyrene oxide, i.e. racemic vicinal diols are produced from the racemic substrates. After saturation mutagenesis
Rainer Gross et al.
Biotechnology and bioengineering, 110(2), 424-436 (2012-08-14)
This study evaluates the technical feasibility of biofilm-based biotransformations at an industrial scale by theoretically designing a process employing membrane fiber modules as being used in the chemical industry and compares the respective process parameters to classical stirred-tank studies. To