1616841-99-6

Basic information

• Product Name: (S)-1-benzyl-N-[4-chloro-2-(2-chlorobenzoyl)phenyl]pyrrolidine-2-carboxamide
• Synonyms: (S)-1-benzyl-N-[4-chloro-2-(2-chlorobenzoyl)phenyl]pyrrolidine-2-carboxamide
• CAS NO: 1616841-99-6
• Molecular Weight: 453.368
• Mol File: 1616841-99-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-1-benzyl-N-[4-chloro-2-(2-chlorobenzoyl)phenyl]pyrrolidine-2-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-benzyl-N-[4-chloro-2-(2-chlorobenzoyl)phenyl]pyrrolidine-2-carboxamide(1616841-99-6)
• EPA Substance Registry System: (S)-1-benzyl-N-[4-chloro-2-(2-chlorobenzoyl)phenyl]pyrrolidine-2-carboxamide(1616841-99-6)

Safety Data

• Hazardous Substances Data: 1616841-99-6(Hazardous Substances Data)

Upstream product

• 31795-93-4 N-benzyl-L-proline 
• 2958-36-3 (2-amino-5-chloro-phenyl)-(2-chloro-phenyl)-methanone 

Relevant articles and documents

Asymmetric synthesis of α-amino acids under operationally convenient conditions

A new multipurpose glycine equivalent for the general asymmetric synthesis of α-amino acids is introduced. The chiral reagent can be transformed to various amino acids by alkylations with alkyl halides as well as aldol and Michael addition reactions under operationally convenient reaction conditions at room temperature with virtually complete stereochemical control.