91110-82-6

Basic information

• Product Name: (E)-1,2-di-(2-phenylphenyl)-ethene
• Synonyms: (E)-1,2-di-(2-phenylphenyl)-ethene
• CAS NO: 91110-82-6
• Molecular Weight: 332.445
• Mol File: 91110-82-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-1,2-di-(2-phenylphenyl)-ethene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1,2-di-(2-phenylphenyl)-ethene(91110-82-6)
• EPA Substance Registry System: (E)-1,2-di-(2-phenylphenyl)-ethene(91110-82-6)

Safety Data

• Hazardous Substances Data: 91110-82-6(Hazardous Substances Data)

Upstream product

• 82214-69-5 2-biphenylmagnesium bromide 
• 1203-68-5 2-Phenylbenzaldehyde 
• 91110-81-5 cis-2,2'-biphenylylstilbene 
• 91110-70-2 {2-[(phenylsulfonyl)methyl]phenyl}benzene 

Relevant articles and documents

Ethylaluminum as an ethylene source for the Mizoroki-Heck-type reaction. Rhodium-catalyzed preparation of stilbene derivatives

Treatment of an organoaluminum reagent bearing aryl and ethyl groups furnishes 1,2-diarylethene derivatives in good to excellent yields by the catalysis of a rhodium complex, in which the ethyl group of the aluminum reagent serves as an ethylene source in the product formation.

Catalytic enantioselective and catalyst-controlled diastereofacial- selective additions of allyl- and crotylboronates to aldehydes using chiral Bronsted acids

(Chemical Equation Presented) Towards the ideal: A chiral diol-SnCl 4 complex is applied to the allylboration of aldehydes (see scheme). This approach highlights the use of chiral Bronsted acid catalysis in the development of an ideal method for the allylation of aldehydes which would display high diastereo- and enantioselectivity, wide substrate scope, and high practicality (ease of use, low cost, and low environmental impact).