6776-31-4

Basic information

• Product Name: 2,2,2-Trifluor-1-acetoxy-N-benzyloxycarbonyl-ethylamin
• Synonyms: 2,2,2-Trifluor-1-acetoxy-N-benzyloxycarbonyl-ethylamin
• CAS NO: 6776-31-4
• Molecular Weight: 291.227
• Mol File: 6776-31-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,2,2-Trifluor-1-acetoxy-N-benzyloxycarbonyl-ethylamin(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,2-Trifluor-1-acetoxy-N-benzyloxycarbonyl-ethylamin(6776-31-4)
• EPA Substance Registry System: 2,2,2-Trifluor-1-acetoxy-N-benzyloxycarbonyl-ethylamin(6776-31-4)

Safety Data

• Hazardous Substances Data: 6776-31-4(Hazardous Substances Data)

Upstream product

• 621-84-1 O-benzyl carbamate 
• 108-24-7 acetic anhydride 
• 433-27-2 ethyl trifluoroacetaldehyde hemiacetal 
• 6798-33-0 1-(benzyloxycarbonylamino)-2,2,2-trifluoroethanol 

Relevant articles and documents

Catalytic Asymmetric Mannich Type Reaction with Tri-/Difluoro- or Trichloroacetaldimine Precursors

A highly efficient catalytic asymmetric Mannich type reaction of CF3-, CF2H-, or CCl3-acetaldimine precursors by a chiral primary amine is presented. This protocol provides facile access to chiral CF3

A chiral α - amino acid derivative and its preparation method (by machine translation)

The invention discloses a chiral α - amino acid derivative and its preparation method. The invention α - chiral amino acid derivatives, its structural formula shown in formula I: Its preparation method, comprises the following steps: with the carbonyl compound to the N, O - acetal of the mixture with a chiral primary uncle diamine organic small molecule catalyst, strong and weak acid mixing, reaction, to obtain the chiral α - amino acid compounds; the carbonyl compound including aldehyde and/or ketone. The invention chiral α - amino acid ester compound having a simple structure of the chiral primary uncle diamine organic small molecule catalyst catalytic, solvent-free, one-step synthesis, simple, high-efficiency. (by machine translation)