119244-26-7

Basic information

• Product Name: tert-butyl (R)-3-(4-chlorophenyl)-2-(diphenylmethanediylamino)propanoate
• Synonyms: tert-butyl (R)-3-(4-chlorophenyl)-2-(diphenylmethanediylamino)propanoate
• CAS NO: 119244-26-7
• Molecular Weight: 419.951
• Mol File: 119244-26-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: tert-butyl (R)-3-(4-chlorophenyl)-2-(diphenylmethanediylamino)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (R)-3-(4-chlorophenyl)-2-(diphenylmethanediylamino)propanoate(119244-26-7)
• EPA Substance Registry System: tert-butyl (R)-3-(4-chlorophenyl)-2-(diphenylmethanediylamino)propanoate(119244-26-7)

Safety Data

• Hazardous Substances Data: 119244-26-7(Hazardous Substances Data)

Upstream product

• 81477-94-3 N-(diphenylmethylene)glycine tert-butyl ester 
• 622-95-7 4-chlorobenzyl bromide 

Downstream Products

• 14091-08-8 para-Chloro-D-phenylalanine 

Relevant articles and documents

Photoswitchable Chiral Phase Transfer Catalyst

Azo-crown ether-based photoswitching chiral phase transfer catalysts have been developed to control the catalytic activity by photoirradiation. Azobenzene binaphthyl crown ether (ABCE) can switch its reactivity and selectivity through structural transform

A new class of acetophenone-based cinchona alkaloids as phase-transfer catalysts: Application to the enantioselective synthesis of α-amino acids

A new class of acetophenone-based cinchona alkaloid-de-rived quaternary ammonium salts were prepared and evaluated as phase-transfer catalysts in the enantioselective alkylation of glycine imine ester. +R 3N-CH2COAr and el

Asymmetric alkylation of glycine imine esters using solid supports preloaded with base

Investigations into the use of solid supports preloaded with base for the asymmetric alkylation of a benzophenone-derived glycine-imine was described. Residual traces of water on the support dramatically accelerated the reactions to complete within a few