105780-05-0

Basic information

• Product Name: (3S,4R)-1-Benzyl-3-((R)-1-hydroxy-ethyl)-4-((E)-styryl)-azetidin-2-one
• CAS NO: 105780-05-0
• Molecular Weight: 307.392
• Mol File: 105780-05-0.mol

Chemical Properties

• CAS DataBase Reference: (3S,4R)-1-Benzyl-3-((R)-1-hydroxy-ethyl)-4-((E)-styryl)-azetidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4R)-1-Benzyl-3-((R)-1-hydroxy-ethyl)-4-((E)-styryl)-azetidin-2-one(105780-05-0)
• EPA Substance Registry System: (3S,4R)-1-Benzyl-3-((R)-1-hydroxy-ethyl)-4-((E)-styryl)-azetidin-2-one(105780-05-0)

Safety Data

• Hazardous Substances Data: 105780-05-0(Hazardous Substances Data)

Upstream product

• 60293-41-6 N-((E)-3-phenylallylidene)benzylamine 
• 105780-02-7 (E)-3-Benzylamino-2-((R)-1-hydroxy-ethyl)-5-phenyl-pent-4-enethioic acid S-phenyl ester 

Relevant articles and documents

ON THE STEREOCHEMICAL COURSE OF VINYLOXYBORANE-IMINE CONDENSATION - THE STEREOSELECTIVE FORMATION OF THREO β-AMINO ACID DERIVATIVES

While reaction of Z(O)-vinyloxyboranes with aldehydes gives erythro aldols highly selectively, it has been found that condensation of Z(O)-vinyloxyboranes with imines provides threo β-amino acid derivatives in a highly selective manner.