16112-20-2

Basic information

• Product Name: 3,5-di(4′-methylphenyl)isoxazole
• Synonyms: 3,5-di(4′-methylphenyl)isoxazole
• CAS NO: 16112-20-2
• Molecular Weight: 249.312
• Mol File: 16112-20-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3,5-di(4′-methylphenyl)isoxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-di(4′-methylphenyl)isoxazole(16112-20-2)
• EPA Substance Registry System: 3,5-di(4′-methylphenyl)isoxazole(16112-20-2)

Safety Data

• Hazardous Substances Data: 16112-20-2(Hazardous Substances Data)

Upstream product

• 10403-54-0 phenyl (3-phenyl-2H-aziren-2-yl)methanone 
• 29559-24-8 4-chlorophenylnitromethane 
• 21551-47-3 4,4'-Dimethylchalcon 
• 104-87-0 4-methyl-benzaldehyde 
• 874-60-2 4-methyl-benzoyl chloride 
• 766-97-2 4-n-methylphenylacetylene 
• 97691-66-2 1,3-bis(4-methylphenyl)prop-2-yn-1-one 
• 32046-98-3 p-tolyl(3-p-tolyloxiran-2-yl)methanone 
• 32045-75-3 4,4'-Dimethylchalane dibromide 
• 20821-96-9 3,5-bis(4-methylphenyl)-2-isoxazoline 
• 29559-27-1 1-methyl-4-(nitromethyl)benzene 
• 3594-36-3 1,3-bis(p-methylphenyl)-1,3-propanedione 

Downstream Products

• 85231-83-0 p-Tolyl-(4-p-tolyl-[1,2,5]thiadiazol-3-yl)-methanone 
• 16178-29-3 3,5-bis-(4-trans-styryl-phenyl)-isoxazole 

Relevant articles and documents

One-pot three-component synthesis of 3,5-disubstituted isoxazoles by a coupling-cyclocondensation sequence

A convenient one-pot procedure for the synthesis of 3,5-disubstituted isoxazoles from acid chloride, terminal alkyne, and hydroxylamine hydrochloride catalyzed by Pd(PPh3)2Cl2/CuI has been developed. The coupling of acid c

Formation of 4-Benzamidoisoxazole Derivatives

The titled compounds (3) were synthesized by the reaction of nitrile oxides with 1-azirines and also the reaction of aliphatic nitro compounds with dibenzoylmethane derivatives in the presence of acetyl chloride and sodium methoxide.The structure of 3 was