1277191-97-5

Basic information

• Product Name: (S)-tert-butyl N-(2,2-difluoro-3-oxo-1,3-diphenylpropyl)carbamate
• Synonyms: (S)-tert-butyl N-(2,2-difluoro-3-oxo-1,3-diphenylpropyl)carbamate
• CAS NO: 1277191-97-5
• Molecular Weight: 361.388
• Mol File: 1277191-97-5.mol

Chemical Properties

• CAS DataBase Reference: (S)-tert-butyl N-(2,2-difluoro-3-oxo-1,3-diphenylpropyl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-tert-butyl N-(2,2-difluoro-3-oxo-1,3-diphenylpropyl)carbamate(1277191-97-5)
• EPA Substance Registry System: (S)-tert-butyl N-(2,2-difluoro-3-oxo-1,3-diphenylpropyl)carbamate(1277191-97-5)

Safety Data

• Hazardous Substances Data: 1277191-97-5(Hazardous Substances Data)

Upstream product

• 13735-81-4 1-styrenyloxytrimethylsilane 
• 86340-78-5 2,2-difluoro-1-phenyl-1-trimethylsiloxyethene 
• 150884-50-7 benzaldehyde N-boc imine 

Downstream Products

• 1277192-13-8 (S)-tert-butyl N-(2-(phenoxycarbonyl)-2,2-difluoro-1-phenylethyl)carbamate 
• 1277192-16-1 (S)-3-amino-2,2-difluoro-1,3-diphenylpropan-1-one 
• 252681-07-5 (4S)-3,3-difluoro-4-phenylazetidin-2-one 

Relevant articles and documents

Chiral phosphoric acid catalyzed enantioselective synthesis of β-amino-α,α-difluoro carbonyl compounds

A biphenol-based chiral phosphoric acid bearing a 9-anthryl group at each of the 3,3′-positions catalyzed the asymmetric Mannich-type reaction of N-Boc imine with difluoroenol silyl ethers in the presence of MS3A in THF to afford β-amino-α,α-difluoroketon