137661-29-1

Basic information

• Product Name: N-methyl-N-(3,5-diphenyl-4-isoxazolylmethyl)hydroxylamine
• Synonyms: N-methyl-N-(3,5-diphenyl-4-isoxazolylmethyl)hydroxylamine
• CAS NO: 137661-29-1
• Molecular Weight: 280.326
• Mol File: 137661-29-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-methyl-N-(3,5-diphenyl-4-isoxazolylmethyl)hydroxylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-methyl-N-(3,5-diphenyl-4-isoxazolylmethyl)hydroxylamine(137661-29-1)
• EPA Substance Registry System: N-methyl-N-(3,5-diphenyl-4-isoxazolylmethyl)hydroxylamine(137661-29-1)

Safety Data

• Hazardous Substances Data: 137661-29-1(Hazardous Substances Data)

Upstream product

• 92859-53-5 4-bromomethyl-3,5-diphenylisoxazole 
• 593-77-1 N-Methylhydroxylamine 

Downstream Products

• 137661-27-9 N-<1-benzoyl-2-(methylamino)ethenyl>benzamide 
• 137661-26-8 2-benzoyl-3-(methylamino)-N-phenylacrylamide 
• 137661-24-6 2,5-dibenzoyl-2,5-di(benzoylamino)-1,4-dimethylpiperazine 
• 2039-49-8 3,5-diphehylisoxazole 
• 92-71-7 2,5-diphenyloxazole 

Relevant articles and documents

Photoreactivity of 4-nucleophile-substituted isoxazoles

The photoreactivity of 1a-1c under steady-state irradiation has been examined and the photoproducts characterized.Several heterocycloes were obtained: 1a gave the pyrrazolines 6 and 7 and the triazine 8; 1b yielded the azetidine 9 and the imidazole 10; 1c gave the imidazole 10, the piperazine 15, the aziridine 16 and the pyrazole 19.In addition, open-chain products were obtained, i.e., the methylaminovinyl ketone 12 from 1b and the enaminones 17 and 18 from 1c.While the formation of most of the products can be explained via the expected intermediate ketenimines, azirines and nitrile ylides, new pathways are involved in the formation of the isoxazole 13 and the pyrazole 19 from 1c