1054513-15-3

Basic information

• Product Name: (2S,5S,1'S)-5-[1-(2-benzyloxybenzoylamino)-2-hydroxyethyl]-1-methylpyrrolidine-2-carboxylic acid tert-butyl ester
• Synonyms: (2S,5S,1'S)-5-[1-(2-benzyloxybenzoylamino)-2-hydroxyethyl]-1-methylpyrrolidine-2-carboxylic acid tert-butyl ester
• CAS NO: 1054513-15-3
• Molecular Weight: 454.566
• Mol File: 1054513-15-3.mol

Chemical Properties

• CAS DataBase Reference: (2S,5S,1'S)-5-[1-(2-benzyloxybenzoylamino)-2-hydroxyethyl]-1-methylpyrrolidine-2-carboxylic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,5S,1'S)-5-[1-(2-benzyloxybenzoylamino)-2-hydroxyethyl]-1-methylpyrrolidine-2-carboxylic acid tert-butyl ester(1054513-15-3)
• EPA Substance Registry System: (2S,5S,1'S)-5-[1-(2-benzyloxybenzoylamino)-2-hydroxyethyl]-1-methylpyrrolidine-2-carboxylic acid tert-butyl ester(1054513-15-3)

Safety Data

• Hazardous Substances Data: 1054513-15-3(Hazardous Substances Data)

Upstream product

• 1054513-13-1 (2S,5S,1'S)-5-[(2-benzyloxybenzoylamino)-ethoxycarbonylmethyl]-1-methylpyrrolidine-2-carboxylic acid tert-butyl ester 

Downstream Products

• 1054513-23-3 C₁₉H₂₈N₂O₅ 

Relevant articles and documents

Synthesis of carbapyochelins via diastereoselective azidation of 5-(ethoxycarbonyl)methylproline derivatives

(Chemical Equation Presented) Two configurationally stable carbon-based analogues of pyochelin have been prepared from Boc-pyroglutamic acid-tert-butyl ester in 11 and 13 steps. Introduction of the amino group was achieved by a highly diastereoselective electrophilic azidation reaction to afford novel bis-α-amino acid proline derivatives.