496790-43-3

Basic information

• Product Name: L-Phenylalanine, 2-bromo-N-(diphenylmethylene)-, 1,1-dimethylethyl ester
• CAS NO: 496790-43-3
• Molecular Formula: C26H26BrNO2
• Molecular Weight: 464.402
• Mol File: 496790-43-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: L-Phenylalanine, 2-bromo-N-(diphenylmethylene)-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Phenylalanine, 2-bromo-N-(diphenylmethylene)-, 1,1-dimethylethyl ester(496790-43-3)
• EPA Substance Registry System: L-Phenylalanine, 2-bromo-N-(diphenylmethylene)-, 1,1-dimethylethyl ester(496790-43-3)

Safety Data

• Hazardous Substances Data: 496790-43-3(Hazardous Substances Data)

Upstream product

• 81477-94-3 N-(diphenylmethylene)glycine tert-butyl ester 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 

Downstream Products

• 79815-20-6 (S)-indoline-2-carboxylic acid 
• 557797-02-1 (S)-2-{[bis-(4-methoxyphenyl)-methylene]-amino}-3-(2-bromophenyl)-propionic acid tert-butyl ester 
• 533902-93-1 (S)-tert-butyl N-acetyl-2-bromophenylalaninate 
• 557796-87-9 (S)-2-amino-3-(2-bromophenyl)-propionic acid tert-butyl ester 
• 496790-47-7 1-benzhydryl-2,3-dihydro-1H-indole-2-carboxylic acid tert-butyl ester 

Relevant articles and documents

Improved access to chiral tetranaphthoazepinium-based organocatalysts using aqueous ammonia as nitrogen source

The class of 3,30-diaryl substituted tetranaphthobisazepinium bromides has found wide application as highly efficient C2-symmetrical phase-transfer catalysts (PTCs, Maruoka type catalysts). Unfortunately, the synthesis requires a lar

Design of N-spiro C2-symmetric chiral quaternary ammonium bromides as novel chiral phase-transfer catalysts: Synthesis and application to practical asymmetric synthesis of α-amino acids

A series of C2-symmetric chiral quaternary ammonium bromides 10 and 11 have been designed as a new, purely synthetic chiral phase-transfer catalyst, and readily prepared from commercially available optically pure 1,1′-bi-2-naphthol as a basic c