103204-83-7

Basic information

• Product Name: 2-oxo-2-(2,5-dimethylphenyl)acetic acid
• Synonyms: 2-oxo-2-(2,5-dimethylphenyl)acetic acid
• CAS NO: 103204-83-7
• Molecular Weight: 178.188
• Mol File: 103204-83-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-oxo-2-(2,5-dimethylphenyl)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-oxo-2-(2,5-dimethylphenyl)acetic acid(103204-83-7)
• EPA Substance Registry System: 2-oxo-2-(2,5-dimethylphenyl)acetic acid(103204-83-7)

Safety Data

• Hazardous Substances Data: 103204-83-7(Hazardous Substances Data)

Upstream product

• 106-42-3 para-xylene 
• 79-37-8 oxalyl dichloride 
• 553-94-6 4-bromo-m-xylene 
• 80120-31-6 ethyl 2-(2,5-dimethylphenyl)-2-oxoacetate 
• 2142-73-6 1-(2,5-dimethylphenyl)-1-ethanone 

Downstream Products

• 1173692-57-3 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazole]-1-piperidinyl]-2-(2,5-dimethylphenyl)-1,2-ethanedione 
• 610-72-0 2,5-dimethylbenzoic acid 
• 124-38-9 carbon dioxide 
• 5779-94-2 2,5-dimethylbenzaldehyde 

Relevant articles and documents

Copper-catalyzed direct α-ketoesterification of propiophenones with acetophenones via C(sp3)-H oxidative cross-coupling

A novel copper-catalyzed direct α-ketoesterification of propiophenones with acetophenones via C(sp3)-H oxidative cross-coupling was developed. The reaction utilized O2 as a clean oxidant with high atom economy and the starting materials are facile and commercially available.

FUNGICIDAL HETERCYCLIC COMPOUNDS

Disclosed are compounds of Formula (1), including all geometric and stereoisomers, N-oxides, and salts thereof, formula (1) wherein E, R2, G, Z1, J and n are as defined in the disclosure. Also disclosed are compositions containing th