1000026-12-9

Basic information

• Product Name: (R,R)-2-[1-(4-bromophenyl)-2-phenyl-but-3-enylamino]-phenol
• Synonyms: (R,R)-2-[1-(4-bromophenyl)-2-phenyl-but-3-enylamino]-phenol
• CAS NO: 1000026-12-9
• Molecular Weight: 394.311
• Mol File: 1000026-12-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R,R)-2-[1-(4-bromophenyl)-2-phenyl-but-3-enylamino]-phenol(CAS DataBase Reference)
• NIST Chemistry Reference: (R,R)-2-[1-(4-bromophenyl)-2-phenyl-but-3-enylamino]-phenol(1000026-12-9)
• EPA Substance Registry System: (R,R)-2-[1-(4-bromophenyl)-2-phenyl-but-3-enylamino]-phenol(1000026-12-9)

Safety Data

• Hazardous Substances Data: 1000026-12-9(Hazardous Substances Data)

Upstream product

• 1000026-07-2 C₁₉H₂₂ClNOSi 
• 117649-27-1 (E)-N-(4-bromobenzylidene)-2-hydroxyaniline 
• 100-42-5 styrene 
• 447440-43-9 (4S,5S)-2-allyl-2-chloro-3,4-dimethyl-5-phenyl-1,3,2-oxazasilolidine 

Relevant articles and documents

Allylsilane-vinylarene cross-metathesis enables a powerful approach to enantioselective imine allylation

Cinnamylation-flavored synthesis: Cross-metathesis (CM) reactions between an allylsilane andvinylarenes enable the rapidgeneration of various cinnamylsilanes, which may be usedin situ for the highly enantioselective, and diastereodivergent, cinnamylation of imines (see example in scheme). Under this new, simple, and efficient protocol, the potential of imine cinnamylation to produce stereochemically andfunctionally complex products has been more fully realized. Ar = thienyl, Ar′ = 2-hydroxyphenyl. (Chemical Equation Presented).