1452311-06-6

Basic information

• Product Name: (Z)-N-benzyl-2-bromo-N'-hydroxybenzimidamide
• Synonyms: (Z)-N-benzyl-2-bromo-N'-hydroxybenzimidamide
• CAS NO: 1452311-06-6
• Molecular Weight: 305.174
• Mol File: 1452311-06-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (Z)-N-benzyl-2-bromo-N'-hydroxybenzimidamide(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-N-benzyl-2-bromo-N'-hydroxybenzimidamide(1452311-06-6)
• EPA Substance Registry System: (Z)-N-benzyl-2-bromo-N'-hydroxybenzimidamide(1452311-06-6)

Safety Data

• Hazardous Substances Data: 1452311-06-6(Hazardous Substances Data)

Upstream product

• 6630-33-7 ortho-bromobenzaldehyde 
• 38435-47-1 2-bromo N-hydroxybenzimidoyl chloride 
• 100-46-9 benzylamine 
• 34158-72-0 2-bromobenzaldehyde oxime 

Downstream Products

• 827332-78-5 3-(2-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.