135395-16-3

Basic information

• Product Name: N-tert-Butyl-N^α-phthaloyl-β-bromophenylalaninamide
• CAS NO: 135395-16-3
• Molecular Weight: 429.313
• Mol File: 135395-16-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-tert-Butyl-N^α-phthaloyl-β-bromophenylalaninamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-tert-Butyl-N^α-phthaloyl-β-bromophenylalaninamide(135395-16-3)
• EPA Substance Registry System: N-tert-Butyl-N^α-phthaloyl-β-bromophenylalaninamide(135395-16-3)

Safety Data

• Hazardous Substances Data: 135395-16-3(Hazardous Substances Data)

Upstream product

• 135395-13-0 (S)-N-(tert-Butyl)-N^α-phthaloylphenylalaninamide 
• 56271-33-1 3-phenyl-2-(phthalimido)propanoyl chloride 
• 3588-64-5 N-phthaloylphenylalanine 
• 135501-56-3 (RS)-N-(tert-Butyl)-N^α-phthaloylphenylalaninamide 

Downstream Products

• 135395-13-0 (S)-N-(tert-Butyl)-N^α-phthaloylphenylalaninamide 
• 160648-63-5 (S)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-3-phenyl-propionamide 
• 6254-48-4 (2S,3R)-3-phenylserine 
• 160648-48-6 (2S,3R)-3-hydroxy-N-t-butyl-N^α-phthaloylphenylalaninamide 

Relevant articles and documents

Regioselective Functionalization of N-Phthaloyl-Substituted Amino Acid and Peptide Derivatives

The free-radical reactions of a range of amino acid derivatives with N-bromosuccinimide are described.The products and relative rates of these reactions indicate that the α-position of an N-phthaloyl-substituted α-amino acid derivative is much less reacti