128156-28-5

Basic information

• Product Name: 5(4H)-Isoxazolone, 4-[(3,4-dimethoxyphenyl)methylene]-3-methyl-
• CAS NO: 128156-28-5
• Molecular Formula: C13H13NO4
• Molecular Weight: 247.251
• Mol File: 128156-28-5.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 5(4H)-Isoxazolone, 4-[(3,4-dimethoxyphenyl)methylene]-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 5(4H)-Isoxazolone, 4-[(3,4-dimethoxyphenyl)methylene]-3-methyl-(128156-28-5)
• EPA Substance Registry System: 5(4H)-Isoxazolone, 4-[(3,4-dimethoxyphenyl)methylene]-3-methyl-(128156-28-5)

Safety Data

• Hazardous Substances Data: 128156-28-5(Hazardous Substances Data)

Upstream product

• 141-97-9 ethyl acetoacetate 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 5447-76-7 ethyl 3-oxobutanate oxime 

Downstream Products

• 6302-60-9 4-(3,4-dimethoxy-phenyl)-butan-2-one 
• 128156-51-4 4,4'-Bis-(3,4-dimethoxy-benzyl)-3,3'-dimethyl-4H,4'H-[4,4']biisoxazolyl-5,5'-dione 
• 128156-34-3 4-(3,4-Dimethoxy-benzyl)-3-methyl-2H-isoxazol-5-one 

Relevant articles and documents

Greener Synthesis of 3,4-Disubstituted Isoxazole-5(4H)-ones in a Deep Eutectic Solvent

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Pyruvic acid-catalyzed one-pot three-component green synthesis of isoxazoles in aqueous medium: a comparable study of conventional heating versus ultra-sonication

A mild and efficient route for the one-pot synthesis of isoxazole derivatives has been developed using pyruvic acid as a catalyst under an aqueous medium. The reaction was carried out under conventional as well as ultrasonic conditions to afford the desir

A simple and efficient protocol for the synthesis of 3,4-disubstituted isoxazol-5(4h)-ones catalyzed by succinic acid using water as green reaction medium

A simple and efficient protocol has been established to the synthesis of 3,4-disubstituted isoxazol-5(4H)-ones via Knoevenagel condensation reaction. In this synthesis, succinic acid was used as an inexpensive catalyst and water as a green reaction medium