51933-59-6

Basic information

• Product Name: Acetic acid, bis(benzoylamino)-, ethyl ester
• CAS NO: 51933-59-6
• Molecular Formula: C18H18N2O4
• Molecular Weight: 326.352
• Mol File: 51933-59-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Acetic acid, bis(benzoylamino)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, bis(benzoylamino)-, ethyl ester(51933-59-6)
• EPA Substance Registry System: Acetic acid, bis(benzoylamino)-, ethyl ester(51933-59-6)

Safety Data

• Hazardous Substances Data: 51933-59-6(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 72761-72-9 bis-benzoylamino-acetic acid 
• 7647-01-0 hydrogenchloride 
• 55-21-0 benzamide 
• 28130-07-6 N-benzoylhydroxyglycine ethyl ester 
• 924-44-7 glyoxylic acid ethyl ester 
• 39593-81-2 N-benzoyl-S-chloro-thiohydroxylamine 
• 1011-57-0 N-trimethylsilylbenzamide 
• 19791-95-8 α-hydroxyhippuric acid 
• 51933-56-3 N-Benzoyl-α-chlor-α-carboethoxymethansulfenamid 

Relevant articles and documents

Bismuth- and Iron-Catalyzed Three-Component Synthesis of α-Amino Acid Derivatives: A Simple and Convenient Route to α-Arylglycines

Efficient bismuth- and iron-catalyzed three-component syntheses of α-arylglycines have been developed. These methods provide a general, atom-economic route to various N-protected α-arylglycines starting from readily available amides (or carbamates), glyoxalates, and (hetero)arenes with water as the only by-product. Scope and limitations of bismuth- and iron-catalyzed reactions are discussed and compared. In addition, mechanistic investigations as well as initial forays into stereoselective three-component reactions are presented.