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
Canonical 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
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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