36954-12-8

Basic information

• Product Name: N-(3-methylphenyl)-benzylamine oxime
• Synonyms: N-(3-methylphenyl)-benzylamine oxime
• CAS NO: 36954-12-8
• Molecular Weight: 226.278
• Mol File: 36954-12-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-(3-methylphenyl)-benzylamine oxime(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-methylphenyl)-benzylamine oxime(36954-12-8)
• EPA Substance Registry System: N-(3-methylphenyl)-benzylamine oxime(36954-12-8)

Safety Data

• Hazardous Substances Data: 36954-12-8(Hazardous Substances Data)

Upstream product

• 100-47-0 benzonitrile 
• 100-52-7 benzaldehyde 
• 932-90-1 Benzaldoxime 
• 698-16-8 benzohydroximoyl chloride 
• 108-44-1 1-amino-3-methylbenzene 
• 52379-50-7 N-(3-methylphenyl)-benzamidine 

Downstream Products

• 76551-71-8 (C₄H₉)3SnOBONC(NC₆H₄CH₃-3)C₆H₅ 
• 76551-72-9 2-triphenylstannoxy-3-m-tolyl-4-phenyl-1,3,5,2-oxadiazaborole 
• 76541-31-6 2,2'-oxybis-3-m-tolyl-4-phenyl-1,3,5,2-oxadiazoborole 
• 7420-86-2 5-methyl-2-phenyl-1,3-benzoxazole 
• 125421-36-5 7-methyl-2-phenylbenzo[d]oxazole 
• 76541-21-4 2-ethoxy-3-m-tolyl-4-phenyl-1,3,5,2-oxadiazaborole 
• 76541-32-7 3,5-diphenyl-4-(m-tolyl)-4,5-dihydro-1,2,4,5-oxadiazaborole 
• 2963-65-7 5-methyl-2-phenyl-1H-1,3-benzimidazole 

Relevant articles and documents

Iodine Promoted One-Pot Synthesis of 2-Aryl Benzoxazoles from Amidoximes via Oxidative Cyclization and Ring Contraction

A molecular I2-promoted one-pot synthesis of 2-aryl benzoxazoles has been developed by using amidoximes rather than the limited 2-aminophenols or 2-haloamides as substrates. The amidoxime substrates provided unique and efficient strategies for converting readily available aniline and benzaldehyde precursors into valuable chemicals. This transformation proceeded smoothly under transition-metal-free conditions through a sequential oxidative cyclization and ring contraction, and provided a potential route for introducing certain groups at any site of the scaffold.

FeCl3·6H2O-mediated reaction of [60]fullerene with amidoximes

A FeCl3·6H2O-mediated reaction of [60]fullerene with amidoximes for the preparation of fulleroimidazolines has been presented. This reaction shows a wide substrate scope, and the products obtained from alkyl-substituted amidoximes ar