957828-79-4

Basic information

• Product Name: [5-(3,4-dichlorophenyl)-3-(2-nitrophenyl)-4,5-dihydroisoxazol-4-yl](phenyl)methanone
• Synonyms: [5-(3,4-dichlorophenyl)-3-(2-nitrophenyl)-4,5-dihydroisoxazol-4-yl](phenyl)methanone
• CAS NO: 957828-79-4
• Molecular Weight: 441.27
• Mol File: 957828-79-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [5-(3,4-dichlorophenyl)-3-(2-nitrophenyl)-4,5-dihydroisoxazol-4-yl](phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: [5-(3,4-dichlorophenyl)-3-(2-nitrophenyl)-4,5-dihydroisoxazol-4-yl](phenyl)methanone(957828-79-4)
• EPA Substance Registry System: [5-(3,4-dichlorophenyl)-3-(2-nitrophenyl)-4,5-dihydroisoxazol-4-yl](phenyl)methanone(957828-79-4)

Safety Data

• Hazardous Substances Data: 957828-79-4(Hazardous Substances Data)

Upstream product

• 35447-75-7 N-hydroxy-2-nitrobenzimidoyl chloride 
• 22966-16-1 3-(3,4-dichlorophenyl)-1-phenyl-2-propen-1-one 

Relevant articles and documents

A general approach to the synthesis of substituted isoxazolo[4,3-c] quinolines via chalcones

A general and practical approach to the synthesis of substituted isoxazolo[4,3-c]quinolines from the substituted isoxazolines obtained by 1,3-dipolar cycloadditions between 2-nitrobenzonitrile oxide and chalcones is described. SnCl2·2H2O-mediated reduction of the nitro group, followed by intramolecular cyclization involving the amino and the keto groups in these substrates, furnished mixtures of isoxazolo[4,3-c] quinolines and 3,5-dihydroisoxazolo[4,3-c]-quinolines. In contrast, the reduction of these substrates with Fe/AcOH unexpectedly yielded 3-benzoylquinolin-4-yl-amine derivatives. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.