3488-57-1

Basic information

• Product Name: N-hydroxy-N-phenyl-benzenecarboximidamide
• CAS NO: 3488-57-1
• Molecular Formula: C₁₃H₁₂N₂O
• Molecular Weight: 212.251
• Mol File: 3488-57-1.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 374.6°Cat760mmHg
• Flash Point: 180.4°C
• Density: 1.1g/cm³
• CAS DataBase Reference: N-hydroxy-N-phenyl-benzenecarboximidamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-hydroxy-N-phenyl-benzenecarboximidamide(3488-57-1)
• EPA Substance Registry System: N-hydroxy-N-phenyl-benzenecarboximidamide(3488-57-1)

Safety Data

• Hazardous Substances Data: 3488-57-1(Hazardous Substances Data)

Upstream product

• 873-67-6 benzonitrile oxide 
• 62-53-3 aniline 
• 1527-91-9 N-phenylbenzamidine 
• 60-29-7 diethyl ether 
• 64-17-5 ethanol 
• 7803-49-8 hydroxylamine 
• 4903-36-0 N-phenyl-benzimidoyl chloride 
• 636-04-4 N-Phenylbenzothioamide 
• 98-88-4 benzoyl chloride 
• 93-98-1 N-phenyl benzoyl amide 
• 932-90-1 Benzaldoxime 
• 100-52-7 benzaldehyde 
• 698-16-8 benzohydroximoyl chloride 

Downstream Products

• 3164-28-1 6-nitro-2-phenylbenzo[d]oxazole 
• 1527-91-9 N-phenylbenzamidine 
• 14562-00-6 (3,4-diphenyl-4H-[1,2,4]oxadiazol-5-ylidene)-phenyl-amine 
• 93-98-1 N-phenyl benzoyl amide 
• 76541-36-1 2-triphenylstannoxy-3-phenyl-4-phenyl-1,3,5,2-oxadiazaborole 
• 102-07-8 bis(diphenyl)urea 
• 14562-01-7 3,4-diphenyl-1,2,4-oxadiazol-5(4H)-one 
• 833-50-1 2-phenylbenzo[d]oxazole 
• 1427216-60-1 C₇₃H₁₀N₂ 
• 64671-56-3 3,4-diphenyl-1,2,4-oxadiazole-5(4H)-thione 
• 5319-63-1 2-phenyl-3-phenyl-4-phenyl-1,3,5,2-oxadiazoborole 

Relevant articles and documents

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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