1133322-57-2

Basic information

• Product Name: 4-(3-methoxy-4,5-methylenedioxyphenyl)-5-methyl-3-(2,4,6-trimethylphenyl)-4,5-dihydroisoxazole
• CAS NO: 1133322-57-2
• Molecular Weight: 353.418
• Mol File: 1133322-57-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-(3-methoxy-4,5-methylenedioxyphenyl)-5-methyl-3-(2,4,6-trimethylphenyl)-4,5-dihydroisoxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3-methoxy-4,5-methylenedioxyphenyl)-5-methyl-3-(2,4,6-trimethylphenyl)-4,5-dihydroisoxazole(1133322-57-2)
• EPA Substance Registry System: 4-(3-methoxy-4,5-methylenedioxyphenyl)-5-methyl-3-(2,4,6-trimethylphenyl)-4,5-dihydroisoxazole(1133322-57-2)

Safety Data

• Hazardous Substances Data: 1133322-57-2(Hazardous Substances Data)

Upstream product

• 18312-21-5 trans-isomyristicin 
• 2904-57-6 mesitylenecarbonitrile oxide 

Relevant articles and documents

Polyalkoxybenzenes from plant sources 2. Synthesis of isoxazoline analogs of combretastatin from natural allyl(methylenedioxy)methoxybenzenes

A series of analogs of the natural mitostatic agent combretastatin were synthesized by the reaction of nitrile oxides with natural allylbenzenes, such as myristicin, apiol, and dillapiol. The 1,3-dipolar cycloaddition reactions in allylic systems proceed regiospecifically. The reactions with trans isomers of propenylbenzenes, viz., isomyristicin, isoapiol, and isodillapiol, as dipolarophiles produce regioisomers.