1020073-95-3

Basic information

• Product Name: (E)-4-(1,2-diphenylvinyl)benzonitrile
• Synonyms: (E)-4-(1,2-diphenylvinyl)benzonitrile
• CAS NO: 1020073-95-3
• Molecular Weight: 281.357
• Mol File: 1020073-95-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-4-(1,2-diphenylvinyl)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-4-(1,2-diphenylvinyl)benzonitrile(1020073-95-3)
• EPA Substance Registry System: (E)-4-(1,2-diphenylvinyl)benzonitrile(1020073-95-3)

Safety Data

• Hazardous Substances Data: 1020073-95-3(Hazardous Substances Data)

Upstream product

• 2252-32-6 4-cyanophenyldiazonium tetrafluoroborate 
• 501-65-5 diphenyl acetylene 
• 623-00-7 4-bromobenzenecarbonitrile 
• 221006-75-3 1-phenyl-2-phenylethyleneboronic acid pinacol ester 
• 126747-14-6 4-cyanophenylboronic acid 
• 264144-59-4 (Z)-1-(4',4',5',5'-tetramethyl-1’,3’,2’-dioxaborolan-2’-yl)-1,2-diphenylethene 
• 14447-41-7 (E)-1-bromo-1,2-diphenylethene 
• 13440-24-9 anti-1,2-dibromo-1,2-diphenylethane 

Relevant articles and documents

Regioselective Synthesis of α-Functional Stilbenes via Precise Control of Rapid cis- trans Isomerization in Flow

The rapid cis-trans isomerization of α-anionic stilbene was regioselectively controlled by using flow microreactors, and its reaction with various electrophiles was conducted. The reaction time was precisely controlled within milliseconds to seconds at -50 °C to selectively give the cis- or trans-isomer in high yields. This synthetic method in flow was well-applied to synthesize precursors of commercial drug compound, (E)- and (Z)-tamoxifen with high regioselectivity and productivity.

Straightforward iron-catalyzed synthesis of vinylboronates by the hydroboration of alkynes

An iron-catalyzed hydroboration of alkynes to produce vinylboronates has been examined. With a straightforward system composed of iron carbonyls and pinacolborane, good to excellent yields and chemoselectivities were achieved for a variety of alkynes. Cop