77629-83-5

Basic information

• Product Name: ethyl 2-broMo-2-(4-Methoxyphenyl)acetate
• Synonyms: ethyl 2-broMo-2-(4-Methoxyphenyl)acetate
• CAS NO: 77629-83-5
• Molecular Formula: C₁₁H₁₃BrO₃
• Molecular Weight: 273.12312
• Mol File: 77629-83-5.mol
• Article Data: 19

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ethyl 2-broMo-2-(4-Methoxyphenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-broMo-2-(4-Methoxyphenyl)acetate(77629-83-5)
• EPA Substance Registry System: ethyl 2-broMo-2-(4-Methoxyphenyl)acetate(77629-83-5)

Safety Data

• Hazardous Substances Data: 77629-83-5(Hazardous Substances Data)

Upstream product

• 14062-18-1 ethyl p-methoxyphenylacetate 
• 5720-07-0 4-methoxyphenylboronic acid 
• 105-36-2 ethyl bromoacetate 
• 36141-66-9 ethyl 2-hydroxy-2-(4-methoxyphenyl)acetate 
• 40140-16-7 ethyl (p-methoxyphenyl)oxoacetate 
• 100-66-3 methoxybenzene 
• 104-01-8 4-Methoxyphenylacetic acid 
• 64-17-5 ethanol 
• 107445-17-0 ethyl 2-diazo-2-(4-methoxyphenyl) acetate 

Downstream Products

• 131403-77-5 1-<2-(α-ethoxycarbonyl-p-methoxybenzyl)thiophenyl>pyrrole 
• 155908-77-3 p-methoxy-α-<<4-chloro-2-(1H-pyrrol-1-yl)phenyl>thio>phenylacetic acid ethyl ester 
• 155908-80-8 (4-Methoxy-phenyl)-(4-methoxy-2-pyrrol-1-yl-phenylsulfanyl)-acetic acid ethyl ester 
• 155908-76-2 (4-Methoxy-phenyl)-(2-pyrrol-1-yl-4-trifluoromethyl-phenylsulfanyl)-acetic acid ethyl ester 
• 155908-79-5 (2-Chloro-6-pyrrol-1-yl-phenylsulfanyl)-(4-methoxy-phenyl)-acetic acid ethyl ester 
• 155908-78-4 (5-Chloro-2-pyrrol-1-yl-phenylsulfanyl)-(4-methoxy-phenyl)-acetic acid ethyl ester 
• 85607-62-1 3-(4-methoxyphenyl)piperazin-2-one 
• 66504-33-4 (1S,2R)-1-(4-Methoxy-phenyl)-cyclopropane-1,2-dicarboxylic acid diethyl ester 
• 190672-11-8 benzenesulfonyl-(4-methoxy-phenyl)-acetic acid ethyl ester 
• 680617-59-8 ethyl α-(4-methoxy-phenyl)-α-[(4-(1H-pyrrol-1-yl)-3-pyridyl)thio]acetate 
• 287393-03-7 ethyl [4-(hydroxyphenyl)sulfanyl](4-methoxyphenyl)acetate 
• 220529-51-1 (methoxy-phenyl)-(4-nitro-imidazol-1-yl)-acetic acid ethyl ester 
• 152302-86-8 Ethyl α-(diethoxyphosphinyl)-α-(4-methoxyphenyl)acetate 
• 869470-04-2 2-methyl-4-(p-methoxyphenyl)-4H-oxazolin-5-one 

Relevant articles and documents

Bromination of α-Diazo Phenylacetate Derivatives Using Cobalt(II) Bromide

A method for the bromination of α-diazo phenylacetate derivatives using cobalt(II) bromide is described. This bromination reaction features a short reaction time, broad substrate scope, operational simplicity, acid-free conditions, and gram-scalability. (Figure presented.).

Mechanochromic Polymers That Turn Green Upon the Dissociation of Diarylbibenzothiophenonyl: The Missing Piece toward Rainbow Mechanochromism

Mechanochromic polymers, that is, polymers sensitive to mechanical impact, promise great potential for applications in damage sensors. In particular, radical-type mechanochromic polymers, which produce colored radical species in response to mechanical str

Construction of Pyrrolo[1,2-a]indoles via Cobalt(III)-Catalyzed Enaminylation of 1-(Pyrimidin-2-yl)-1H-indoles with Ketenimines and Subsequent Base-Promoted Cyclization

A cobalt(III)-catalyzed cross-coupling reaction of 1-(pyrimidin-2-yl)-1H-indoles with ketenimines is reported. The reaction provided 2-enaminylated indole derivatives in moderate to excellent yields with a broad substrate scope. The prepared 2-enaminylated indoles could be conveniently converted into pyrrolo[1,2-a]indoles, which are an important class of compounds in medicinal chemistry.