2856-79-3

Basic information

• Product Name: Benzeneacetic acid, .alpha.-broMo-2-chloro-, ethyl ester
• Synonyms: Benzeneacetic acid, .alpha.-broMo-2-chloro-, ethyl ester;ethyl 2-bromo-2-(2-chlorophenyl)acetate;ethyl 2-bromo-2-(2-chlorophenyl)acetate(WXC07030)
• CAS NO: 2856-79-3
• Molecular Formula: C₁₀H₁₀BrClO₂
• Molecular Weight: 277.5422
• Mol File: 2856-79-3.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzeneacetic acid, .alpha.-broMo-2-chloro-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, .alpha.-broMo-2-chloro-, ethyl ester(2856-79-3)
• EPA Substance Registry System: Benzeneacetic acid, .alpha.-broMo-2-chloro-, ethyl ester(2856-79-3)

Safety Data

• Hazardous Substances Data: 2856-79-3(Hazardous Substances Data)

Usage

General Description

Benzeneacetic acid, alpha-bromo-2-chloro-, ethyl ester is a chemical compound with the formula C10H10BrClO2. It is an ethyl ester derivative of alpha-bromo-2-chloro-benzoic acid, and is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Benzeneacetic acid, .alpha.-broMo-2-chloro-, ethyl ester is a colorless liquid with a strong and sweet odor, and it is classified as a hazardous substance due to its potential to cause skin and eye irritation, as well as harmful effects if ingested or inhaled. It is important to handle this chemical with caution and in accordance with proper safety protocols.

Upstream product

• 40061-54-9 2-chlorophenylacetic acid ethyl ester 
• 13511-30-3 ethyl 2-(2-chlorophenyl)-2-hydroxyacetate 
• 2444-36-2 2'-chloro-benzeneacetic acid 
• 66985-47-5 2-chloro-α-[(trimethylsilyl)oxy]benzeneacetonitrile 
• 89-98-5 2-chloro-benzaldehyde 
• 1398179-33-3 o-chlorophenyldiazoacetic acid ethyl ester 

Downstream Products

• 151954-50-6 3-<<4-phenyl>methyl>-5,7-dimethyl-2-ethyl-3H-imidazo<4,5-b>pyridine 
• 77053-65-7 (1R,2S)-1-(2-Chloro-phenyl)-cyclopropane-1,2-dicarboxylic acid diethyl ester 
• 111371-21-2 ethyl (+/-)-2-(2-chlorophenyl)-2-(1H-imidazol-1-yl)acetate 
• 141109-25-3 (S)-(+)-2-bromo-2-(2-chlorophenyl)acetic acid 
• 151954-60-8 3-<<4-phenyl>methyl>-5,7-dimethyl-2-ethyl-3H-imidazo<4,5-b>pyridine 
• 58553-47-2 2-(2-chloro-phenyl)-4H-benzo[1,4]thiazin-3-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.).

ANTIMALARIAL AGENTS HAVING POLYAROMATIC STRUCTURE

Antimalarial agents having a novel pharmacophore of formula (I) are herein described. These polycyclic compounds are able to inhibit chloroquine-sensitive and chloroquine-resistant strains ofPlasmodium falciparum (Pf). Furthermore, the synthesis of these compounds involves few steps from commercial products with low cost of production.Λa présente invention concerne des agents antimalariaux comportant un nouveau pharmacophore de formule (I). Ces composés polycycliques sont susceptibles d''inhiber les souches sensibles à la chloroquine et résistantes à la chloroquine de Plasmodium falciparum (Pf). En outre, la synthèse de ces composés est peu onéreuse et implique peu d''étapes à partir des produits commerciaux.

(Dipropylphenoxy)phenylacetic acids: A new generation of nonpeptide angiotensin II receptor antagonists

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