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cis-Stilbenoxid
97%
Synonym(e):
cis-2,3-Diphenyl-oxiran
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About This Item
Empirische Formel (Hill-System):
C14H12O
CAS-Nummer:
Molekulargewicht:
196.24
Beilstein:
82737
MDL-Nummer:
UNSPSC-Code:
12162002
PubChem Substanz-ID:
NACRES:
NA.23
Empfohlene Produkte
Qualitätsniveau
Assay
97%
mp (Schmelzpunkt)
38-40 °C (lit.)
Lagertemp.
2-8°C
SMILES String
O1[C@H]([C@H]1c2ccccc2)c3ccccc3
InChI
1S/C14H12O/c1-3-7-11(8-4-1)13-14(15-13)12-9-5-2-6-10-12/h1-10,13-14H/t13-,14+
InChIKey
ARCJQKUWGAZPFX-OKILXGFUSA-N
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Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
228.2 °F - closed cup
Flammpunkt (°C)
109 °C - closed cup
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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Hesam Arabnejad et al.
Chembiochem : a European journal of chemical biology, 21(13), 1893-1904 (2020-01-22)
The use of enzymes in preparative biocatalysis often requires tailoring enzyme selectivity by protein engineering. Herein we explore the use of computational library design and molecular dynamics simulations to create variants of limonene epoxide hydrolase that produce enantiomeric diols from
Li-Ming Yang et al.
Bioorganic & medicinal chemistry letters, 12(7), 1013-1015 (2002-03-23)
A new series of trans-stilbene benzenesulfonamide derivatives were designed and synthesized as potential antitumor agents. These new compounds were evaluated in the National Cancer Institute's 60 human tumor cell line in vitro screen. Compounds 9-13 were cytotoxic against several cell
V J Mayani et al.
Chirality, 21(2), 255-261 (2008-06-19)
Chromatographic behavior of nonracemic mixtures, viz., mandelic acid and stilbene oxide as analytes has been studied in detailed by enantiomer self-disproportionation on achiral ordered mesoporous material M41S and regular silica gel as stationary phases. Enantiomer self-disproportionation gave enhanced separation of
Rujin Gong et al.
Journal of chromatography. A, 1286, 119-126 (2013-03-19)
The chromatographic enantioseparation of trans-stilbene oxide (TSO) was studied experimentally and theoretically, where the preparative column was packed with 20 μm Chiralcel OD stationary phase and hexanes/2-propanol were used as mobile phase. The bed porosity, axial dispersion coefficient, mass transfer
Larry Miller et al.
Journal of chromatography. A, 1250, 256-263 (2012-06-26)
Preparative supercritical fluid chromatography (SFC) has become the preferred method for the rapid purification of drug candidates during the pharmaceutical discovery process. This paper will discuss the evaluation of injection techniques for preparative SFC. A thorough evaluation of mixed stream
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