76103-94-1

Basic information

• Product Name: 3-(2-methoxy-phenyl)-3-oxo-propionic acid
• Synonyms: 3-(2-methoxy-phenyl)-3-oxo-propionic acid
• CAS NO: 76103-94-1
• Molecular Weight: 194.187
• Mol File: 76103-94-1.mol

Chemical Properties

• CAS DataBase Reference: 3-(2-methoxy-phenyl)-3-oxo-propionic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-methoxy-phenyl)-3-oxo-propionic acid(76103-94-1)
• EPA Substance Registry System: 3-(2-methoxy-phenyl)-3-oxo-propionic acid(76103-94-1)

Safety Data

• Hazardous Substances Data: 76103-94-1(Hazardous Substances Data)

Upstream product

• 7335-26-4 ethyl 2-methoxybenzoate 
• 41607-95-8 3-(2-methoxy-phenyl)-3-oxo-propionic acid ethyl ester 

Downstream Products

• 2967-87-5 2-fluoro-1-(2-methoxyphenyl)ethanone 
• 1533453-05-2 3-cyclohexyl-1-(2-methoxyphenyl)pent-4-en-1-one 
• 1533453-20-1 3-benzyl-1-(2-methoxyphenyl)-3-methylpent-4-en-1-one 
• 442640-18-8 3-hydroxy-3-(2-(2-methoxyphenyl)-2-oxoethyl)indolin-2-one 
• 1447666-77-4 N-(3-(2-methoxyphenyl)-3-oxo-1-phenylpropyl)-4-methylbenzenesulfonamide 
• 1392149-65-3 (3R)-tert-butyl 3-hydroxy-3-(2-(2-methoxyphenyl)-2-oxoethyl)-2-oxo-2,3-dihydro-1H-indoline-1-carboxylate 

Relevant articles and documents

Synthesis of γ-pyrones via decarboxylative condensation of β-ketoacids

Abstract: This manuscript describes the convergent synthesis of aryl- and alkyl-disubstituted γ-pyrones from β-ketoacids. The reaction proceeds in the presence of trifluoromethanesulfonic anhydride via an unprecedented decarboxylative auto-condensation of the starting material. Herein, the scope and limitations of this transformation are reported. Graphical abstract: [Figure not available: see fulltext.]