76670-23-0

Basic information

• Product Name: O-benzimidoylbenzamidoxime
• Synonyms: O-benzimidoylbenzamidoxime
• CAS NO: 76670-23-0
• Molecular Weight: 239.277
• Mol File: 76670-23-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: O-benzimidoylbenzamidoxime(CAS DataBase Reference)
• NIST Chemistry Reference: O-benzimidoylbenzamidoxime(76670-23-0)
• EPA Substance Registry System: O-benzimidoylbenzamidoxime(76670-23-0)

Safety Data

• Hazardous Substances Data: 76670-23-0(Hazardous Substances Data)

Upstream product

• 613-92-3 N-hydroxybenzenecarboximidamide 
• 76670-24-1 O-(N-acetylbenzimidoyl)benzamidoxime 
• 76670-33-2 C₁₄H₁₃N₃O*ClH 

Downstream Products

• 613-92-3 N-hydroxybenzenecarboximidamide 
• 76670-33-2 C₁₄H₁₃N₃O*ClH 
• 1575-95-7 N-acetylbenzamide 
• 942-87-0 N'-acetoxybenzimidamide 
• 10364-68-8 5-ethyl-3-phenyl-[1,2,4]oxadiazole 
• 1198-98-7 5-methyl-3-phenyl-1,2,4-oxadiazole 
• 888-71-1 3,5-diphenyl-1,2,4-oxadiazole 
• 100-47-0 benzonitrile 
• 76670-24-1 O-(N-acetylbenzimidoyl)benzamidoxime 

Relevant articles and documents

Formation and Thermal Reaction of O-(N-Acetylbenzimidoyl)benzamidoxime: Comparison with the Formation of 3,5-Disubstituted 1,2,4-Oxadiazoles from O-Acetylarylamidoximes and O-Aroylacetamidoximes

Salts of O-(benzimidoyl)benzamidoxime have been obtained by the action of N-chloro- or N-bromo-succinimide, or the halogens, on benzamidoxime.Acetylation of the free base gave the title compound, which underwent a thermal cyclisation, with loss of acetamide, to give 3,5-diphenyl-1,2,4-oxadiazole.The mechanism of the reaction, in diphenyl ether, closely paralleled the thermal cyclisation of O-acetylarylamidoximes and O-aroylacetamidoximes, and is thought to involve a polar cyclisation step followed by rate-determining proton transfer. 13C N.m.r. spectra for 32 oxime, amidoxime, O-acetylamidoxime, 5-methyl-1,2,4-oxadiazol-3-yl, and 3-methyl-1,2,4-oxadiazol-5-yl groups on the phenyl ring are calculated.