690260-90-3

Basic information

• Product Name: Ethyl 2-bromo-4-chlorobenzoate
• Synonyms: Ethyl 2-bromo-4-chlorobenzoate
• CAS NO: 690260-90-3
• Molecular Formula: C₉H₈BrClO₂
• Molecular Weight: 263.51562
• Mol File: 690260-90-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 285.1±20.0 °C at 760 mmHg
• Flash Point: 126.2±21.8 °C
• Appearance: /
• Density: 1.5±0.1 g/cm³
• Storage Temp.: Room temperature.
• CAS DataBase Reference: Ethyl 2-bromo-4-chlorobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 2-bromo-4-chlorobenzoate(690260-90-3)
• EPA Substance Registry System: Ethyl 2-bromo-4-chlorobenzoate(690260-90-3)

Safety Data

• Hazardous Substances Data: 690260-90-3(Hazardous Substances Data)

Usage

General Description

Ethyl 2-bromo-4-chlorobenzoate is a chemical compound with the molecular formula C9H8BrClO2. It is a white crystalline solid with a molecular weight of 255.52 g/mol. This chemical is commonly used in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. It is also utilized in the manufacturing of dyes and other fine chemicals. Ethyl 2-bromo-4-chlorobenzoate is considered to be a hazardous chemical and should be handled and stored with proper safety precautions.

Upstream product

• 64-17-5 ethanol 
• 116779-74-9 2-bromo-4-chlorobenzoyl chloride 
• 7335-27-5 ethyl 4-chlorobenzoate 
• 936-08-3 2-bromo-4-chlorobenzoic acid 

Downstream Products

• 690261-06-4 ethyl 5-chloro-2-[(phenylmethyl)-oxy]-1,1';2',1-terphenyl-2-carboxylate 
• 1023334-50-0 2-bromo-4-chlorobenzohydrazide 

Relevant articles and documents

2,3-DIHYDROQUINAZOLIN COMPOUNDS AS NAV1.8 INHIBITORS

The present invention relates to Nav1.8 Inhibitor 2,3-dihydroquinazolin compounds of Formula (X); wherein Y', X', B', R1', R2', R3', R5', R6', R7', and z1 are as defined herein; or pharmaceutically acceptable salts or tautomer forms thereof, corresponding pharmaceutical compositions or formulations, methods or processes of compound preparation, methods, compounds for use in, uses for and/or combination therapies for treating pain and/or pain-related or associated disease(s), disorder(s) or condition(s), respectively.

An efficient and mild ortho-zincation of aromatics and heterocycles by using TMP2Mg·2LiCl in the presence of ZnCl2

A variety range of functionalized aryl and heteroaryl zinc reagents were efficiently generated by using TMP2Mg·2LiCl (TMP = 2,2,6,6-tetramethylpiperamidyl) in the presence of ZnCl2. The subsequently functionalization gave after react