914250-82-1

Basic information

• Product Name: 3-BROMO-2-CHLOROBENZONITRILE
• Synonyms: 3-BROMO-2-CHLOROBENZONITRILE;2-Chloro-3-bromobenzonitrile;Benzonitrile, 3-bromo-2-chloro-
• CAS NO: 914250-82-1
• Molecular Formula: C₇H₃BrClN
• Molecular Weight: 216.47
• Mol File: 914250-82-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 277.9±20.0 °C(Predicted)
• Appearance: /
• Density: 1.74±0.1 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3-BROMO-2-CHLOROBENZONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMO-2-CHLOROBENZONITRILE(914250-82-1)
• EPA Substance Registry System: 3-BROMO-2-CHLOROBENZONITRILE(914250-82-1)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 914250-82-1(Hazardous Substances Data)

Usage

General Description

3-Bromo-2-chlorobenzonitrile is a chemical compound with the molecular formula C7H3BrClN. It is an organic compound that contains both bromine and chlorine atoms attached to a benzene ring with a nitrile functional group. 3-BROMO-2-CHLOROBENZONITRILE is commonly used in the pharmaceutical and agrochemical industries as a building block for the synthesis of various compounds. It is also used as an intermediate in the manufacture of dyes, pigments, and other organic compounds. 3-Bromo-2-chlorobenzonitrile is known to be a hazardous chemical and should be handled with care and in accordance with safety regulations.

Upstream product

• 6952-59-6 3-cyanobromobenzene 

Downstream Products

• 914250-83-2 3-bromo-2-(2-isopropylphenoxy)benzonitrile 
• 914250-84-3 3-bromo-2-(2,4,6-trimethylphenoxy)benzonitrile 
• 1260021-59-7 3-bromo-2-chloro-N-hydroxybenzenecarboximidamide 
• 1036734-36-7 3-bromo-2-(2-tert-butylphenoxy)-benzonitrile 
• 914250-88-7 2-(2,6-diisopropylphenoxy)-3-[(hydroxy)(phenyl)methyl]benzonitrile 

Relevant articles and documents

Hindered diarylether and diarylsulfone bisphosphine ligands: Atropisomerism and palladium complexes

Phosphines and bisphosphines derived from hindered ortho-substituted diaryl ethers and diarylsulfones by lithiation are, with appropriate substitution patterns, resolvable atropisomeric ligands which form crystalline complexes with palladium dichloride.

Three groups good, four groups bad? Atropisomerism in ortho-substituted diaryl ethers

(Chemical Equation Presented) Bring on the substitute: Even outside of macrocyclic structures, such as vancomycin, appropriate substitution can give rise to atropisomerism in diaryl ethers. Stereochemical stability about the Ar-OAr axis at room temperature or above is possible when neither of the rings is symmetrically substituted and when at least one ring carries an ortho tert-butyl group or equivalent.