196928-07-1

Basic information

• Product Name: N-(2-azidobenzoyl)-N-methyl-L-phenylalanine methyl ester
• Synonyms: N-(2-azidobenzoyl)-N-methyl-L-phenylalanine methyl ester
• CAS NO: 196928-07-1
• Molecular Weight: 338.366
• Mol File: 196928-07-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(2-azidobenzoyl)-N-methyl-L-phenylalanine methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-azidobenzoyl)-N-methyl-L-phenylalanine methyl ester(196928-07-1)
• EPA Substance Registry System: N-(2-azidobenzoyl)-N-methyl-L-phenylalanine methyl ester(196928-07-1)

Safety Data

• Hazardous Substances Data: 196928-07-1(Hazardous Substances Data)

Upstream product

• 2439-60-3 N-methyl-L-phenylalanine methyl ester 
• 34897-85-3 o-azidobenzoyl chloride 
• 37553-64-3 (S)-methyl 2-((tert-butoxycarbonyl)(methyl)amino)-3-phenylpropanoate 
• 31162-13-7 2-azidobenzoic acid 

Downstream Products

• 211567-41-8 (3S)-3,4-dihydro-2-methoxy-N-methyl-3-phenylmethyl-[1,4]benzodiazepin-5(5H)one 
• 50886-63-0 (3S)-3,4-dihydro-4-methyl-3-phenylmethyl-[1,4]benzodiazepin-2,5(1H)-dione 
• 196928-08-2 (3S)-[1-(2-azidobenzoyl)]-3,4-dihydro-4-methyl-3-phenylmethyl-[1,4]benzodiazepin-2,5(1H)-dione 
• 157047-96-6 (-)-benzomalvin A 

Relevant articles and documents

Insights into the Desaturation of Cyclopeptin and its C3 Epimer Catalyzed by a non-Heme Iron Enzyme: Structural Characterization and Mechanism Elucidation

AsqJ, an iron(II)- and 2-oxoglutarate-dependent enzyme found in viridicatin-type alkaloid biosynthetic pathways, catalyzes sequential desaturation and epoxidation to produce cyclopenins. Crystal structures of AsqJ bound to cyclopeptin and its C3 epimer ar

The first total synthesis of (-)-benzomalvin A via intramolecular Aza-Wittig reactions

The first total synthesis of (-)-benzomalvin A 1, which possesses quinazolin-4(3H)-one moiety and 1,4-benzodiazepin-5-one moiety, was described. Both of 6- and 7-membered ring skeletons were efficiently constructed by intramolecular aza-Wittig reactions as the key reactions.