95199-89-6

Basic information

• Product Name: Isoxazolo[5,4-b]pyridine-5-carboxylic acid, 4,7-dihydro-3-(4-methoxyphenyl)-6-methyl-4-phenyl-, ethyl ester
• CAS NO: 95199-89-6
• Molecular Formula: C23H22N2O4
• Molecular Weight: 390.439
• Mol File: 95199-89-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Isoxazolo[5,4-b]pyridine-5-carboxylic acid, 4,7-dihydro-3-(4-methoxyphenyl)-6-methyl-4-phenyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Isoxazolo[5,4-b]pyridine-5-carboxylic acid, 4,7-dihydro-3-(4-methoxyphenyl)-6-methyl-4-phenyl-, ethyl ester(95199-89-6)
• EPA Substance Registry System: Isoxazolo[5,4-b]pyridine-5-carboxylic acid, 4,7-dihydro-3-(4-methoxyphenyl)-6-methyl-4-phenyl-, ethyl ester(95199-89-6)

Safety Data

• Hazardous Substances Data: 95199-89-6(Hazardous Substances Data)

Upstream product

• 98516-48-4 5-(2-ethoxycarbonyl-3-oxo-1-phenyl)butylamino-3-phenylisoxazole 
• 86685-98-5 3-(4-methoxyphenyl)-1,2-oxazol-5-amine 
• 620-80-4 ethyl 2-benzylidene acetoacetate 

Relevant articles and documents

STUDIES ON DIHYDROPYRIDINE DERIVATIVES-I 4,7-DIHYDROISOXAZOLOPYRIDINES

Reactions of 5-aminoisoxazoles with α,β-unsaturated ketones in t-butanol on heating afforded 4,7-dihydroisoxazolopyridines.However, when the reactions were carried out at 20 deg C using ethylene glycol as the solvent, the kinetically controlled amino adducts were obtained in excellent yields.The amino adducts were converted into the thermodynamically controlled 4,7-dihydroisoxazolopyridines by heating.Tentative mechanisms for the reaction are also presented.