37613-33-5

Basic information

• Product Name: Isoxazole, 5-(4-methoxyphenyl)-3-(4-methylphenyl)-
• CAS NO: 37613-33-5
• Molecular Formula: C17H15NO2
• Molecular Weight: 265.312
• Mol File: 37613-33-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Isoxazole, 5-(4-methoxyphenyl)-3-(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoxazole, 5-(4-methoxyphenyl)-3-(4-methylphenyl)-(37613-33-5)
• EPA Substance Registry System: Isoxazole, 5-(4-methoxyphenyl)-3-(4-methylphenyl)-(37613-33-5)

Safety Data

• Hazardous Substances Data: 37613-33-5(Hazardous Substances Data)

Upstream product

• 5650-35-1 [3-(4-methoxy-phenyl)-oxiranyl]-p-tolyl-methanone 
• 100945-45-7 1-(4-methoxyphenyl)-2-(4-methylphenyl)cyclopropane 
• 64-17-5 ethanol 
• 25856-03-5 1-(4-methoxy-phenyl)-3-p-tolyl-propane-1,3-dione 
• 7732-18-5 water 
• 6552-66-5 3-(4-methoxyphenyl)-1-p-tolylprop-2-en-1-one 
• 32045-76-4 2,3-dibromo-3-(4-methoxyphenyl)-1-(4-methylphenyl)-propan-1-one 
• 51250-75-0 3-(4-methylphenyl)-5-(4-methoxyphenyl)-4,5-dihydroisoxazole 
• 2089-33-0 4-methylacethophenone oxime 
• 874-90-8 4-methoxybenzonitrile 

Relevant articles and documents

Aerobic oxidative synthesis of 3,5-disubstituted isoxazoles directly from α,β-unsaturated ketones

Using an efficient aerobic oxidative method, the synthesis of ten 3,5-disubstituted isoxazoles by treatment of α,β-unsaturated ketones with hydroxylamine and NaOH at room temperature has been achieved.

BEHAVIOR OF UNSYMMETRICAL 1,2-DIARYLCYCLOPROPANES UNDER THE CONDITIONS OF NITROSATION

Isomeric 3,5-diaryl-4,5-dihydroisoxazoles were obtained as a result of the reaction of unsymmetrical 1,2-diarylcyclopropanes, differing in the nature of substituents in the benzene rings, with sodium nitrite in a mixture of chloroform and trifluoroacetic