41024-33-3

Basic information

• Product Name: ALPHA-BROMO-3-CHLOROBENZENEACETIC ACID ETHYL ESTER
• Synonyms: ALPHA-BROMO-3-CHLOROBENZENEACETIC ACID ETHYL ESTER;Ethyl (alpha-bromo-3-chloro)phenylacetate;Ethyl2-Bromo-2-(3-chlorophenyl)acetate;Ethyl 2-bromo-2-(3-chlorophen-1-yl)acetate;Ethyl bromo(3-chlorophenyl)acetate;ALPHA-BROMO-3-CHLORO-, METHYL ESTER BENZENEACETIC ACID;Benzeneacetic acid,alpha-bromo-3-chloro-ethyl ester;a-Bromo-3-chlorobenz
• CAS NO: 41024-33-3
• Molecular Formula: C₁₀H₁₀BrClO₂
• Molecular Weight: 277.54
• Mol File: 41024-33-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 296.1 °C at 760 mmHg
• Flash Point: 132.9 °C
• Appearance: /
• Density: 1.503 g/cm³
• Vapor Pressure: 0.00146mmHg at 25°C
• Refractive Index: 1.557
• Storage Temp.: 2-8°C
• CAS DataBase Reference: ALPHA-BROMO-3-CHLOROBENZENEACETIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: ALPHA-BROMO-3-CHLOROBENZENEACETIC ACID ETHYL ESTER(41024-33-3)
• EPA Substance Registry System: ALPHA-BROMO-3-CHLOROBENZENEACETIC ACID ETHYL ESTER(41024-33-3)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 41024-33-3(Hazardous Substances Data)

Usage

General Description

Alpha-Bromo-3-Chlorobenzeneacetic Acid Ethyl Ester is a synthetic chemical compound. As the name suggests, this compound carries a bromo and chloro group on a benzene ring along with an ethyl ester group, which is associated with carboxylic acid. The compound is mainly used in organic synthesis and as a precursor for other chemical compounds. It's an aromatic ester with complex properties due to the presence of multiple functional groups. However, more detailed and specific information about its toxicity, health effects, or environmental impact is not readily available, indicating it's not widely used or studied. Precautionary measures and handling guidelines would typically be guided by its Material Safety Data Sheet (MSDS) for those dealing with the compound in a research or industrial setting.

InChI:InChI=1/C10H10BrClO2/c1-2-14-10(13)9(11)7-4-3-5-8(12)6-7/h3-6,9H,2H2,1H3

Upstream product

• 54395-28-7 ethyl 2-(3-chlorophenyl)-2-hydroxyacetate 
• 14062-29-4 ethyl 2-(3-chlorophenyl)acetate 
• 100948-25-2 2-(3-chlorophenyl)-2-(trimethylsilyloxy)acetonitrile 
• 587-04-2 m-Chlorobenzaldehyde 
• 1398179-38-8 ethyl 2-(3-chlorophenyl)-2-diazoacetate 

Downstream Products

• 66503-96-6 (1R,2S)-1-(3-Chloro-phenyl)-cyclopropane-1,2-dicarboxylic acid diethyl ester 
• 869347-30-8 (+/-)-α-(3-chlorophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl ester 
• 946005-77-2 C₁₃H₁₃N₂O₂Cl 
• 946005-78-3 C₁₁H₉N₂O₂Cl 
• 869347-40-0 (+/-)-α-ethyl-α-(3-chlorophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid 
• 869347-35-3 (+/-)-α-ethyl-α-(3-chlorophenyl)-α-[[2-(1H-pyrrol-1-yl)phenyl]oxy]acetic acid ethyl ester 
• 287393-09-3 ethyl (3-chlorophenyl)[(4-hydroxyphenyl)sulfanyl] acetate 
• 1438263-68-3 C₁₅H₁₃ClO₅ 

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.).

Development of piperazine-tethered heterodimers as potent antimalarials against chloroquine-resistant P. falciparum strains. Synthesis and molecular modeling

The design, synthesis, and antiplasmodial activity of antimalarial heterodimers based on the 1,4-bis(3-aminopropyl)piperazine linker is reported. In this series key structural elements derived from quinoline antimalarials were coupled to fragments capable

Method of treating depression using azabicyclohexanes

The present invention concerns certain novel substituted 3-azabicyclo[3.1.0]hexanes and a method of treating depression and stress in a warm-blooded animal, comprising the administration of substituted 3-azabicyclo[3.1.0]hexanes.