128156-33-2

Upstream product

• 17975-46-1 3-methyl-4-(4-methoxyphenyl)methyleneisoxazole-5(4H)-one 
• 36298-56-3 (4Z)-4-(4-methoxybenzylidene)-3-methylisoxazol-5(4H)-one 

Downstream Products

• 104-20-1 4-(4-methoxyphenyl)-2-butanone 
• 51062-15-8 (+)-(R)-1-Methyl-3-(4-methoxyphenyl)-1-propylamine 
• 128156-50-3 4,4'-Bis-(4-methoxy-benzyl)-3,3'-dimethyl-4H,4'H-[4,4']biisoxazolyl-5,5'-dione 
• 141648-73-9 4-(4-Methoxy-benzyl)-3-methyl-2-(3-oxo-butyl)-2H-isoxazol-5-one 
• 141648-69-3 4-(4-Methoxy-benzyl)-3-methyl-4-(3-oxo-butyl)-4H-isoxazol-5-one 
• 141648-54-6 3-[4-(4-Methoxy-benzyl)-3-methyl-5-oxo-5H-isoxazol-2-yl]-propionitrile 
• 141648-49-9 3-[4-(4-Methoxy-benzyl)-3-methyl-5-oxo-4,5-dihydro-isoxazol-4-yl]-propionitrile 
• 136811-25-1 (Z)-3-Benzoylamino-2-(4-methoxy-benzyl)-but-2-enoic acid 
• 138963-80-1 (Z)-2-(4-Methoxy-benzyl)-3-methoxycarbonylamino-but-2-enoic acid 
• 141648-64-8 3-[4-(4-Methoxy-benzyl)-3-methyl-5-oxo-5H-isoxazol-2-yl]-propionic acid ethyl ester 
• 141648-59-1 3-[4-(4-Methoxy-benzyl)-3-methyl-5-oxo-4,5-dihydro-isoxazol-4-yl]-propionic acid ethyl ester 
• 136811-22-8 2-Benzoyl-4-(4-methoxy-benzyl)-3-methyl-2H-isoxazol-5-one 

Relevant academic research and scientific papers

Selective reduction exocyclic double bond of isoxazolones and pyrazolones by hantzsch 1,4-dihydropyridine

Hantzsch 1,4-dihydropyridine (HEH) was used to realize the selective reduction of the exocyclic double bond of 4-arylmethylene- and 4-alkylidene-4H-isoxazol-5-ones and 4-arylraethylene-4H-pyrazol-5-ones. Georg Thieme Verlag Stuttgart.

Chemistry of 5(2H)-Isoxazolones: Novel Conversion of Positional Isomers

Reactions of 4-arylidene-3-methyl-5(4H)-isoxazolones with nucleophiles lead to 4-substituted-benzyl-3-methyl-5(2H)-isoxazolones.Formation of 5(4H)- and 5(2H)-isoxazolone derivatives have been observed when 4-substituted-arylidene-3-methyl-5(4H)-isoxazolon