105780-02-7

Basic information

• Product Name: (E)-3-Benzylamino-2-((R)-1-hydroxy-ethyl)-5-phenyl-pent-4-enethioic acid S-phenyl ester
• CAS NO: 105780-02-7
• Molecular Weight: 417.572
• Mol File: 105780-02-7.mol

Chemical Properties

• CAS DataBase Reference: (E)-3-Benzylamino-2-((R)-1-hydroxy-ethyl)-5-phenyl-pent-4-enethioic acid S-phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-Benzylamino-2-((R)-1-hydroxy-ethyl)-5-phenyl-pent-4-enethioic acid S-phenyl ester(105780-02-7)
• EPA Substance Registry System: (E)-3-Benzylamino-2-((R)-1-hydroxy-ethyl)-5-phenyl-pent-4-enethioic acid S-phenyl ester(105780-02-7)

Safety Data

• Hazardous Substances Data: 105780-02-7(Hazardous Substances Data)

Upstream product

• 60293-41-6 N-((E)-3-phenylallylidene)benzylamine 

Downstream Products

• 105780-05-0 (3S,4R)-1-Benzyl-3-((R)-1-hydroxy-ethyl)-4-((E)-styryl)-azetidin-2-one 

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.