1452311-23-7

Basic information

• Product Name: (Z)-N-benzyl-4-bromo-N'-hydroxybenzimidamide
• Synonyms: (Z)-N-benzyl-4-bromo-N'-hydroxybenzimidamide
• CAS NO: 1452311-23-7
• Molecular Weight: 305.174
• Mol File: 1452311-23-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (Z)-N-benzyl-4-bromo-N'-hydroxybenzimidamide(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-N-benzyl-4-bromo-N'-hydroxybenzimidamide(1452311-23-7)
• EPA Substance Registry System: (Z)-N-benzyl-4-bromo-N'-hydroxybenzimidamide(1452311-23-7)

Safety Data

• Hazardous Substances Data: 1452311-23-7(Hazardous Substances Data)

Upstream product

• 1122-91-4 4-bromo-benzaldehyde 
• 100-46-9 benzylamine 
• 29203-58-5 4-bromo-N-hydroxybenzenecarboximidoyl chloride 
• 25062-46-8 4-bromobenzaldehyde oxime 

Downstream Products

• 65004-19-5 3-(4-bromophenyl)-5-phenyl[1,2,4]oxadiazole 

Relevant articles and documents

Electrochemical synthesis of 1,2,4-oxadiazoles from amidoximes through dehydrogenative cyclization

A convenient and efficient method for the generation of the iminoxy radical through anodic oxidation was developed for the synthesis of 3,5-disubstituted 1,2,4-oxadiazoles fromN-benzyl amidoximes. The transformation proceeds through 1.5-Hydrogen Atom Transfer (1,5-HAT) and intramolecular cyclization. The process features simple operation, mild conditions, broad substrate scope and high functional group compatibility, and provides a facile and practical way for the preparation of 1,2,4-oxadiazoles.