CIS-STILBENE OXIDE
Product Information
Molecular Formula
C14H12O
Molecular Weight
196.24
Description
Cis-stilbene oxide is a stilbene oxide.
Synonyms
Oxirane, 2,3-diphenyl-, cis-; Oxirane,cis-2,3-diphenyl-; CIS-STILBENE OXIDE; cis-2,3-diphenyloxirane; (2R,3S)-2,3-Diphenyloxirane; (2S,3R)-2,3-Diphenyloxirane; meso-Stilbene oxide; Bibenzyl, .alpha.,.alpha.'-epoxy-, cis-
IUPAC Name
(2R,3S)-2,3-diphenyloxirane
SMILES
C1=CC=C(C=C1)C2C(O2)C3=CC=CC=C3
InChI
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+
InChI Key
ARCJQKUWGAZPFX-OKILXGFUSA-N
Melting Point
38-40 °C (lit.)
Purity
0.97
Storage
2-8°C
Computed Properties
XLogP3
2.9
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
2
Exact Mass
196.088815002 g/mol
Monoisotopic Mass
196.088815002 g/mol
Topological Polar Surface Area
12.5Ų
Heavy Atom Count
15
Formal Charge
0
Complexity
179
Isotope Atom Count
0
Defined Atom Stereocenter Count
2
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113908788-A | Biomass pretreatment method based on electromigration effect | 2021-10-08 |
| KR-20210041861-A | Catalyst for preparing cyclic carbonates and manufacturing cyclic carbonates | 2019-10-08 |
| CN-112300842-A | Demulsifier for fuel containing quaternary ammonium salt | 2019-07-23 |
| EP-3770234-A1 | Demulsifier for quaternary ammonium salt containing fuels | 2019-07-23 |
| KR-20210012916-A | Demulsifier for quaternary ammonium salt containing fuels | 2019-07-23 |
| US-2021024844-A1 | Demulsifier for quaternary ammonium salt containing fuels | 2019-07-23 |
| US-11008526-B2 | Demulsifier for quaternary ammonium salt containing fuels | 2019-07-23 |
| US-2020287240-A1 | Carbon Fiber Battery Electrodes With Ionic Liquid and Gel Electrolytes | 2019-03-04 |
| KR-102109645-B1 | Manganese(â…¢)-iodosylbenzene complex, preparation method thereof and oxidant comprising the same | 2019-01-29 |
| JP-2020055769-A | Method for synthesizing sodium silyl compound and method for deoxidizing epoxy compound | 2018-10-01 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 22727558 | 2012-08-10 | Evaluation of injection conditions for preparative supercritical fluid chromatography | Journal of chromatography. A |
| 22280021 | 2012-02-27 | Determinants of reactivity and selectivity in soluble epoxide hydrolase from quantum mechanics/molecular mechanics modeling | Biochemistry |
| 22191979 | 2012-01-11 | An electric field-induced change in the selectivity of a metal oxide-catalyzed epoxide rearrangement | Journal of the American Chemical Society |
| 21798545 | 2011-09-16 | A test to determine the nature and presence of the memory effect columns packed with the amylose tris(3,5-dimethylphenylcarbamate) stationary phase | Journal of chromatography. A |
| 21726877 | 2011-08-05 | The influence of the memory effect on preparative separations using the amylose tris(3,5-dimethylphenylcarbamate) stationary phase | Journal of chromatography. A |
| 21371418 | 2011-07-01 | Development of fluorescent substrates for microsomal epoxide hydrolase and application to inhibition studies | Analytical biochemistry |
| 21455491 | 2011-03-01 | A Pseudomonas aeruginosa toxin that hijacks the host ubiquitin proteolytic system | PLoS pathogens |
| 21125689 | 2011-01-01 | Enantioselective desymmetrization of meso-epoxides with anilines catalyzed by polymeric and monomeric Ti(IV) salen complexes | Chirality |
| 20565054 | 2010-07-19 | Modular, active, and robust Lewis acid catalysts supported on a metal-organic framework | Inorganic chemistry |
| 20132598 | 2010-01-01 | Temporal and spatial resolution in transmission Raman spectroscopy | Applied spectroscopy |
