511544-23-3

Basic information

• Product Name: (S)-N-(2-benzoylphenyl)-1-(2,3,4,5,6-pentafluorobenzyl)pyrrolidine-2-carboxamide
• CAS NO: 511544-23-3
• Molecular Weight: 474.43
• Mol File: 511544-23-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-N-(2-benzoylphenyl)-1-(2,3,4,5,6-pentafluorobenzyl)pyrrolidine-2-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-(2-benzoylphenyl)-1-(2,3,4,5,6-pentafluorobenzyl)pyrrolidine-2-carboxamide(511544-23-3)
• EPA Substance Registry System: (S)-N-(2-benzoylphenyl)-1-(2,3,4,5,6-pentafluorobenzyl)pyrrolidine-2-carboxamide(511544-23-3)

Safety Data

• Hazardous Substances Data: 511544-23-3(Hazardous Substances Data)

Upstream product

• 67-63-0 isopropyl alcohol 
• 653-35-0 2,3,4,5,6-pentafluorobenzyl chloride 
• 2835-77-0 (2-aminophenyl)(phenyl)methanone 
• 147-85-3 L-proline 

Relevant articles and documents

Halo-substituted (S)-N-(2-benzoylphenyl)-1-benzylpyrolidine-2-carboxamides as new chiral auxiliaries for the asymmetric synthesis of (S)-α-amino acids

The synthesis of new chiral auxiliaries (S)-N-(2-benzoylphenyl)-1-(3,4-dichlorobenzyl)-pyrrolidine-2-carboxamide (1a), (S)-N-(2-benzoylphenyl)-1-(pentafluorobenzyl)pyrrolidine-2-carboxamide (1b), and (S)-N-(2-benzoylphenyl)-1-(4-isopropoxytetrafluorobenzyl) pyrrolidine-2-carboxamide (1c) and their application in the asymmetric synthesis of amino acids using NiII complexes of their Schiff's bases with alanine and glycine are described. Compound la is particularly appropriate for highly stereoselective synthesis of α-methyl-α -amino acids with high enatiomeric purity (ee >95%).