57179-42-7

Basic information

• Product Name: ethyl 3-acetyl-4-methyl-2-oxo-6-phenylpyridine-5-carboxylate
• Synonyms: ethyl 3-acetyl-4-methyl-2-oxo-6-phenylpyridine-5-carboxylate
• CAS NO: 57179-42-7
• Molecular Weight: 299.326
• Mol File: 57179-42-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 3-acetyl-4-methyl-2-oxo-6-phenylpyridine-5-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-acetyl-4-methyl-2-oxo-6-phenylpyridine-5-carboxylate(57179-42-7)
• EPA Substance Registry System: ethyl 3-acetyl-4-methyl-2-oxo-6-phenylpyridine-5-carboxylate(57179-42-7)

Safety Data

• Hazardous Substances Data: 57179-42-7(Hazardous Substances Data)

Upstream product

• 95199-75-0 ethyl 3,4-dimethyl-6-phenyl-4,7-dihydroisoxazolo<5,4-b>pyridine-5-carboxylate 
• 39626-32-9 2-benzoyl-but-2-enoic acid ethyl ester 
• 98516-47-3 ethyl 3,4-dimethyl-6-phenylisoxazolo<5,4-b>pyridine-5-carboxylate 

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.