1286741-82-9

Basic information

• Product Name: (E)-5-(4-methylstyryl)-10,11-dihydro-5H-dibenzo[a,d][7]annulene
• Synonyms: (E)-5-(4-methylstyryl)-10,11-dihydro-5H-dibenzo[a,d][7]annulene
• CAS NO: 1286741-82-9
• Molecular Weight: 310.439
• Mol File: 1286741-82-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-5-(4-methylstyryl)-10,11-dihydro-5H-dibenzo[a,d][7]annulene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-5-(4-methylstyryl)-10,11-dihydro-5H-dibenzo[a,d][7]annulene(1286741-82-9)
• EPA Substance Registry System: (E)-5-(4-methylstyryl)-10,11-dihydro-5H-dibenzo[a,d][7]annulene(1286741-82-9)

Safety Data

• Hazardous Substances Data: 1286741-82-9(Hazardous Substances Data)

Upstream product

• 536-50-5 CH₃C₆H₄CH(CH₃)OH 
• 1210-34-0 dibenzosuberol 

Relevant articles and documents

Iron-catalyzed stereospecific olefin synthesis by direct coupling of alcohols and alkenes with alcohols

Chemical equations presented. An efficient Fe(III)-catalyzed direct coupling of alkenes with alcohols and cross-coupling of alcohols with alcohols to give the corresponding substituted (E)-alkenes stereospecifically is demonstrated. Additionally, this reaction could be scaled up. The kinetic isotope effect (KIE) experiments indicated a typical secondary isotope effect in this process. Although benzylic alcohols were effective substrates, mild conditions, atom efficiency, environmental soundness, and stereospecificity are features that make this procedure very attractive.