84325-97-3

Basic information

• Product Name: methyl 2-(4-acetylphenyl)propanoate
• Synonyms: methyl 2-(4-acetylphenyl)propanoate
• CAS NO: 84325-97-3
• Molecular Weight: 206.241
• Mol File: 84325-97-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 2-(4-acetylphenyl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(4-acetylphenyl)propanoate(84325-97-3)
• EPA Substance Registry System: methyl 2-(4-acetylphenyl)propanoate(84325-97-3)

Safety Data

• Hazardous Substances Data: 84325-97-3(Hazardous Substances Data)

Upstream product

• 17639-93-9 2-chloro-propionic acid methyl ester 
• 99-90-1 para-bromoacetophenone 
• 67-56-1 methanol 
• 112921-88-7 1-(4-(prop-1-yn-1-yl)phenyl)ethan-1-one 

Downstream Products

• 84326-11-4 2-[4-(6-Nitro-2-oxo-2H-benzo[1,4]oxazin-3-yl)-phenyl]-propionic acid methyl ester 
• 84326-13-6 2-[4-(6,8-Dimethyl-2-oxo-2H-benzo[1,4]oxazin-3-yl)-phenyl]-propionic acid methyl ester 
• 84326-09-0 2-[4-(6-Chloro-2-oxo-2H-benzo[1,4]oxazin-3-yl)-phenyl]-propionic acid methyl ester 
• 84326-12-5 2-[4-(8-Chloro-2-oxo-2H-benzo[1,4]oxazin-3-yl)-phenyl]-propionic acid methyl ester 
• 84326-10-3 2-[4-(6-Methyl-2-oxo-2H-benzo[1,4]oxazin-3-yl)-phenyl]-propionic acid methyl ester 
• 84326-08-9 Methyl 4-(2H-1,4-benzoxazin-2-one-3-yl)phenyl-α-methylacetate 
• 84326-01-2 2-(4-Ethoxyoxalyl-phenyl)-propionic acid methyl ester 
• 84325-99-5 2-[4-(2-Bromo-acetyl)-phenyl]-propionic acid methyl ester 
• 41387-29-5 2-[4-(acetyl)phenyl] propanoic acid 

Relevant articles and documents

Oxidative Rearrangement of Alkynes to Carboxylic Acid Esters by benzene in Methanol

A direct synthesis of methyl aryl alkanoate via oxidative rearrangement of alkynes using benzene in methanol is described.

Ni-catalyzed activation of α-chloroesters: a simple method for the synthesis of α-arylesters and β-hydroxyesters

Coupling reactions of α-chloroesters with aryl halides (α-arylation) or carbonyl compounds (Reformatsky) using nickel catalyst allow, under mild conditions, the preparation of various functionalized aryl propionic acid derivatives or β-hydroxyesters. In the synthesis of aryl propionic acid derivatives, the process is efficient with aryl halides bearing either electron-withdrawing or electron-donating groups.