76008-75-8

Basic information

• Product Name: Benzoic acid, 3-broMo-4-chloro-, ethyl ester
• Synonyms: Benzoic acid, 3-broMo-4-chloro-, ethyl ester;3-Bromo-4-chloro-benzoic acid ethyl ester
• CAS NO: 76008-75-8
• Molecular Formula: C₉H₈BrClO₂
• Molecular Weight: 263.51562
• Mol File: 76008-75-8.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Benzoic acid, 3-broMo-4-chloro-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3-broMo-4-chloro-, ethyl ester(76008-75-8)
• EPA Substance Registry System: Benzoic acid, 3-broMo-4-chloro-, ethyl ester(76008-75-8)

Safety Data

• Hazardous Substances Data: 76008-75-8(Hazardous Substances Data)

Usage

General Description

Benzoic acid, 3-bromo-4-chloro-, ethyl ester is a chemical compound with the molecular formula C9H8BrClO2. It is an ester of benzoic acid, containing both bromine and chlorine atoms. Benzoic acid, 3-bromo-4-chloro-, ethyl ester is commonly used as a flavoring agent in food and beverages due to its pleasant aroma and taste. It is also used as a preservative in cosmetics and personal care products. Additionally, it has potential applications in the pharmaceutical industry, particularly in the synthesis of pharmaceutical intermediates. Despite its useful properties, it is important to handle this chemical with care, as it can be irritating to the skin, eyes, and respiratory system.

Upstream product

• 64-17-5 ethanol 
• 42860-10-6 3-bromo-4-chlorobenzoic acid 
• 75-03-6 ethyl iodide 
• 74-11-3 para-chlorobenzoic acid 

Downstream Products

• 1008529-57-4 4-chloro-3-(3,3-dimethylbutyl)benzoic acid ethyl ester 
• 329218-12-4 3-bromo-4-chloro-benzyl alcohol 
• 1350629-02-5 ethyl 1,2-diphenyl-1H-benzo[d]imidazole-5-carboxylate 
• 1616603-73-6 ethyl 1-benzyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-5-carboxylate 
• 17518-97-7 trans-6-bromo-7-chloro-3-(3-(3-hydroxypiperidine-2-yl)-2-oxopropyl)quinazolin-4(3H)-one hydrobromide 
• 17518-95-5 6-bromo-7-chloroquinazolin-4(3H)-one 

Relevant articles and documents

A convergent strategy towards febrifugine and related compounds

We report a modular five step synthetic route to the febrifugines that employs 2-(chloromethyl)allyl-trimethylsilane as a conjunctive reagent for the coupling of the piperidine and quinazolinone groups. We also demonstrate the application of a recent Rh-catalyzed quinazolinone synthesis for the facile generation of febrifugine analogs.

INDAZOLE DERIVATIVES THAT INHIBIT TRPV1 AND USES THEREOF

Compounds of formula (I) wherein R3, R7, R9 and L are defined in the description are TRPV1 antagonists that exhibit low inhibitory activity against CYP3A4. Compositions comprising such compounds and methods for treating co

Heterocyclic derivatives for the treatment of diabetes and other diseases

The present invention relates to certain substituted heterocycles of Formula (I) which are useful in the treatment of diseases related to lipid and carbohydrate metabolism, such as type 2 diabetes, adipocyte differentiation, uncontrolled proliferation, such as lymphoma, Hodgkin's Disease, leukemia, breast cancer, prostate cancer or cancers in general; and inflammation, such as osteoarthritis, rheumatoid arthritis, Crohn's Disease or Inflammatory Bowel Disease.