1370701-00-0

Basic information

• Product Name: (E)-1-(2-bromophenyl)-3-phenylprop-2-en-1-ol
• Synonyms: (E)-1-(2-bromophenyl)-3-phenylprop-2-en-1-ol
• CAS NO: 1370701-00-0
• Molecular Weight: 289.172
• Mol File: 1370701-00-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-1-(2-bromophenyl)-3-phenylprop-2-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(2-bromophenyl)-3-phenylprop-2-en-1-ol(1370701-00-0)
• EPA Substance Registry System: (E)-1-(2-bromophenyl)-3-phenylprop-2-en-1-ol(1370701-00-0)

Safety Data

• Hazardous Substances Data: 1370701-00-0(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 114837-50-2 2-bromo-α-(ethenyl)benzenemethanol 
• 300657-41-4 (E)-1-(2-bromophenyl)-3-phenylprop-2-en-1-one 
• 2142-69-0 2-bromophenyl methyl ketone 

Relevant articles and documents

Beyond the Corey–Chaykovsky Reaction: Synthesis of Unusual Cyclopropanoids via Desymmetrization and Thereof

Desymmetrization-based protocols for the synthesis of highly functionalized indeno-spirocyclopropanes and cyclopropa-fused indanes have been established through unexpected reactions triggered by the Corey–Chaykovsky reagent. These structures were further elaborated in one step to privileged scaffolds such as fluorenones, indenones, and naphthaphenones. For instance, an acid-catalyzed transformation of indeno-spirocyclopropanes provided fluorenones via a homo-Nazarov-type cyclization, and naphthaphenones were obtained via an acid-catalyzed cyclopropane ring-opening/retro-Michael sequence.