146933-25-7

Basic information

• Product Name: 3-(4-methoxyphenyl)-5-phenyl-4,5-dihydroisoxazol-5-ol
• Synonyms: 3-(4-methoxyphenyl)-5-phenyl-4,5-dihydroisoxazol-5-ol
• CAS NO: 146933-25-7
• Molecular Weight: 269.3
• Mol File: 146933-25-7.mol

Chemical Properties

• CAS DataBase Reference: 3-(4-methoxyphenyl)-5-phenyl-4,5-dihydroisoxazol-5-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methoxyphenyl)-5-phenyl-4,5-dihydroisoxazol-5-ol(146933-25-7)
• EPA Substance Registry System: 3-(4-methoxyphenyl)-5-phenyl-4,5-dihydroisoxazol-5-ol(146933-25-7)

Safety Data

• Hazardous Substances Data: 146933-25-7(Hazardous Substances Data)

Upstream product

• 6327-79-3 1-(4-methoxyphenyl)-3-phenylpropane-1,3-dione 
• 5739-38-8 1-(4-methoxyphenyl)-3-phenylpropan-1-one 
• 959-33-1 3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one 

Downstream Products

• 3672-52-4 3-(4-methoxyphenyl)-5-phenylisoxazole 

Relevant articles and documents

Metal-free cascade synthesis of unsymmetrical 2-aminopyrimidines from imidazolate enaminones

A convenient metal-free synthesis of unsymmetrical 2-aminopyrimidines from imidazolate enaminones has been developed. In this procedure, various structural 2-aminopyrimidines, as well as 4,5-dihydroisoxazol-5-ols and pyrazoles were synthesized in moderate to excellent yields. A plausible mechanism was also proposed for the cascade reaction. This method represents an effective strategy towards the synthesis of unsymmetrical 2-aminopyrimidines.

TEMPO-Mediated Selective Synthesis of Isoxazolines, 5-Hydroxy-2-isoxazolines, and Isoxazoles via Aliphatic δ-C(sp3)-H Bond Oxidation of Oximes

Selective synthesis of three different bioactive heterocycles; isoxazolines, 5-hydroxy-2-isoxazolines and isoxazoles from the same starting material using TEMPO (2,2,6,6-Tetramethylpiperidin-1-oxyl) as a radical initiator is reported. Selectivity was achi

Efficient and regioselective synthesis of 5-hydroxy-2-isoxazolines: Versatile synthons for isoxazoles, β-lactams, and γ-amino alcohols

"Chemical Equation Presented" An efficient and highly regioselective protocol was developed for the preparation of 5-hydroxy2-isoxazolines, which have been proved to be versatile synthons for isoxazles, β-hydroxy oximes, and γ-amino alcohols. β-Lactams, commonly embedded in the skeletons of bioactive natural products, were also synthesized in two steps from β-hydroxy oximes, providing a new strategy for the synthesis of this kind of compounds.

On the Oximation of Diaryl-β-diketones

The reaction of asymmetrically substituted β-diketones with hydroxylamine to give 3,5-diarylisoxazoles has been re-investigated, and has been found to occur with a low degree of site-selectivity unless steric effects are operating.The isoxazole that has t