1566556-29-3

Basic information

• Product Name: (S)-P,P-diphenyl-N-(1-phenylbuta-2,3-dien-1-yl)phosphinic amide
• Synonyms: (S)-P,P-diphenyl-N-(1-phenylbuta-2,3-dien-1-yl)phosphinic amide
• CAS NO: 1566556-29-3
• Molecular Weight: 345.381
• Mol File: 1566556-29-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-P,P-diphenyl-N-(1-phenylbuta-2,3-dien-1-yl)phosphinic amide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-P,P-diphenyl-N-(1-phenylbuta-2,3-dien-1-yl)phosphinic amide(1566556-29-3)
• EPA Substance Registry System: (S)-P,P-diphenyl-N-(1-phenylbuta-2,3-dien-1-yl)phosphinic amide(1566556-29-3)

Safety Data

• Hazardous Substances Data: 1566556-29-3(Hazardous Substances Data)

Upstream product

• 1566556-27-1 (R)-P,P-diphenyl-N-(1-phenyl-2-(trimethylsilyl)buta-2,3-dien-1-yl)phosphinic amide 
• 1337935-39-3 4,4,5,5-tetramethyl-2-(prop-2-yn-1-yl)-1,3,2-dioxaborolane 
• 98837-46-8 P,P-diphenyl-N-(phenylmethylene)phosphinic amide 

Relevant articles and documents

NHC-Cu-catalyzed addition of propargylboron reagents to phosphinoylimines. Enantioselective synthesis of trimethylsilyl-substituted homoallenylamides and application to the synthesis of S-(-)-cyclooroidin

A catalytic method for the efficient and enantioselective addition of a 1-trimethylsilyl-substituted allene moiety to phosphinoylimines is presented. Transformations are promoted by 5.0 mol % of a copper complex of an N-heterocyclic carbene in the presenc