793728-14-0

Basic information

• Product Name: 2-amino-3-[3-(7-bromo-2-oxo-3-phenyl-2,3-dihydro-1H-indol-3-yl)-4-hydroxy-phenyl]-propionic acid methyl ester
• Synonyms: 2-amino-3-[3-(7-bromo-2-oxo-3-phenyl-2,3-dihydro-1H-indol-3-yl)-4-hydroxy-phenyl]-propionic acid methyl ester
• CAS NO: 793728-14-0
• Molecular Weight: 481.346
• Mol File: 793728-14-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-amino-3-[3-(7-bromo-2-oxo-3-phenyl-2,3-dihydro-1H-indol-3-yl)-4-hydroxy-phenyl]-propionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-3-[3-(7-bromo-2-oxo-3-phenyl-2,3-dihydro-1H-indol-3-yl)-4-hydroxy-phenyl]-propionic acid methyl ester(793728-14-0)
• EPA Substance Registry System: 2-amino-3-[3-(7-bromo-2-oxo-3-phenyl-2,3-dihydro-1H-indol-3-yl)-4-hydroxy-phenyl]-propionic acid methyl ester(793728-14-0)

Safety Data

• Hazardous Substances Data: 793728-14-0(Hazardous Substances Data)

Upstream product

• 615-36-1 2-bromoaniline 
• 20780-74-9 7-bromoisatin 
• 63220-44-0 7-bromo-3-hydroxy-3-phenyl-1,3-dihydroindol-2-one 
• 2440-79-1 N-acetyl-L-tyrosine methyl ester 
• 13512-31-7 N-(benzyloxycarbonyl)-L-tyrosine methyl ester 

Downstream Products

• 496789-41-4 2-acetylamino-3-[3-(7-bromo-2-oxo-3-phenyl-2,3-dihydro-1H-indol-3-yl)-4-hydroxy-phenyl]-propionic acid methyl ester 

Relevant articles and documents

Chemistry and biology of diazonamide A: First total synthesis and confirmation of the true structure

With the addition of a tenth ring, the exchange of an oxygen atom for a nitrogen in the heart of the molecule, and a different terminal residue, the revised architecture for diazonamide A (1) provided an even more challenging molecular puzzle for chemical synthesis than its predecessor. In this article, we detail the first successful total synthesis of diazonamide A, an endeavor which not only verified its proper connectivities and established the stereochemistry of its previously unassignable C-37 chiral center, but which also was attended by the development of several new synthetic strategies and tactics.