135395-13-0

Basic information

• Product Name: (S)-N-(tert-Butyl)-N^α-phthaloylphenylalaninamide
• Synonyms: (S)-N-(tert-Butyl)-N^α-phthaloylphenylalaninamide
• CAS NO: 135395-13-0
• Molecular Weight: 350.417
• Mol File: 135395-13-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-N-(tert-Butyl)-N^α-phthaloylphenylalaninamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-(tert-Butyl)-N^α-phthaloylphenylalaninamide(135395-13-0)
• EPA Substance Registry System: (S)-N-(tert-Butyl)-N^α-phthaloylphenylalaninamide(135395-13-0)

Safety Data

• Hazardous Substances Data: 135395-13-0(Hazardous Substances Data)

Upstream product

• 135395-16-3 N-tert-Butyl-N^α-phthaloyl-β-bromophenylalaninamide 
• 5123-55-7 Nα-phthaloyl-L-phenylalanine 
• 63-91-2 L-phenylalanine 
• 85-44-9 phthalic anhydride 
• 75-64-9 tert-butylamine 
• 32150-91-7 phthaloyl-L-phenylalanyl chloride 

Downstream Products

• 135395-16-3 N-tert-Butyl-N^α-phthaloyl-β-bromophenylalaninamide 
• 160648-48-6 (2S,3R)-3-hydroxy-N-t-butyl-N^α-phthaloylphenylalaninamide 
• 753487-93-3 (S)-2-{[(S)-2-((2S,3R)-2-tert-Butoxycarbonylamino-3-methoxy-3-phenyl-propionylamino)-3-methyl-butyryl]-methyl-amino}-4-methyl-pentanoic acid allyl ester 
• 753487-75-1 (S)-2-{[(S)-2-((2S,3R)-2-Amino-3-methoxy-3-phenyl-propionylamino)-3-methyl-butyryl]-methyl-amino}-4-methyl-pentanoic acid allyl ester 
• 753487-59-1 (2S,3R)-3-methoxy-N-tert-butyl-N²-phthaloylphenylalanylamide 
• 855315-37-6 (2S,3R)-N-(tert-butyloxycarbonyl)-3-methoxyphenylalanine methyl ester 
• 753487-55-7 (2S,3R)-N-(tert-butyloxycarbonyl)-3-methoxyphenylalanine 
• 753488-03-8 2-amino-N-tert-butyl-3-methoxy-3-phenyl-propionamide 
• 874894-76-5 (2S,3R)-2-amino-3-methoxy-3-phenylpropanoic acid 

Relevant articles and documents

Total synthesis of cyclomarin C

The total synthesis of cyclomarin C was accomplished through a convergent strategy from a tetrapeptide fragment and a tripeptide one. The developed methods to prepare the needed noncoded amino acids, the proper protection of peptide fragments, and identification of the optimum macrocylization site can be applied to further synthetic studies on other members of cyclomarins.