85875
trans-Stilbene oxide
purum, ≥98.0% (HPLC)
Synonym(s):
trans-1,2-Diphenyloxirane
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About This Item
Empirical Formula (Hill Notation):
C14H12O
CAS Number:
Molecular Weight:
196.24
EC Number:
215-877-7
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
82740
MDL number:
InChI key
ARCJQKUWGAZPFX-ZIAGYGMSSA-N
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-/m1/s1
SMILES string
O1[C@@H]([C@H]1c2ccccc2)c3ccccc3
grade
purum
assay
≥98.0% (HPLC)
mp
65-67 °C (lit.), 66-69 °C
Other Notes
This product has been replaced by S4921-ALDRICH | trans-Stilbene oxide 98%
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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
Neil Everall et al.
Applied spectroscopy, 64(1), 52-60 (2010-02-06)
Picosecond time-resolved transmission Raman data were acquired for 1 mm thick powder samples of trans-stilbene, and a Monte Carlo model was developed that can successfully model the laser and Raman pulse profiles. Photon migration broadened the incident (approximately 1 ps)
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
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
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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