42860-16-2

Basic information

• Product Name: 2-Bromo-5-chlorobenzoyl chloride
• Synonyms: 2-Bromo-5-chlorobenzoyl chloride
• CAS NO: 42860-16-2
• Molecular Formula: C₇H₃BrCl₂O
• Molecular Weight: 253.90812
• Mol File: 42860-16-2.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Bromo-5-chlorobenzoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-5-chlorobenzoyl chloride(42860-16-2)
• EPA Substance Registry System: 2-Bromo-5-chlorobenzoyl chloride(42860-16-2)

Safety Data

• Hazard Codes: C
• Hazardous Substances Data: 42860-16-2(Hazardous Substances Data)

Upstream product

• 21739-93-5 2-bromo-5-chlorobenzoic acid 
• 2516-95-2 5-chloro-2-nitrobenzoic acid 
• 14495-51-3 2-bromo-5-chlorotoluene 

Downstream Products

• 96463-49-9 2-bromo-5,3'-dichloro-benzophenone 
• 835-09-6 (2-bromo-5-chlorophenyl)(phenyl)methanone 
• 924660-37-7 N-benzyl-2-bromo-5-chlorobenzamide 
• 100397-76-0 2-benzyl-1-bromo-4-chlorobenzene 
• 96583-68-5 1-bromo-4-chloro-2-(3-chlorobenzyl)benzene 
• 105901-09-5 (2-bromo-5-chlorophenyl)(phenyl)methanol 
• 96462-70-3 (2-bromo-5-chlorophenyl)(3-chlorophenyl)methanol 
• 1338379-18-2 (Z)-2-benzyl-6-chloro-3-(phenylmethylene)isoindolin-1-one 
• 1381842-11-0 C₁₇H₁₅BrClNO₅ 
• 1578240-44-4 2-bromo-5-chlorobenzoyl ferrocene 
• 849106-18-9 2-(2-bromo-5-chloro-phenyl)-4,4-dimethyl-4,5-dihydro-oxazole 
• 849106-19-0 4-[4-chloro-2-(4,4-dimethyl-4,5-dihydro-oxazol-2-yl)-phenyl]-4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester 

Relevant articles and documents

Targeting the Kv11.1 (hERG) channel with allosteric modulators. Synthesis and biological evaluation of three novel series of LUF7346 derivatives

We synthesized and evaluated three novel series of substituted benzophenones for their allosteric modulation of the human Kv11.1 (hERG) channel. We compared their effects with reference compound LUF7346 previously shown to shorten the action po

Copper-Catalyzed Cascade Synthesis of [1,2,4]-Triazoloquinazolinones

An efficient and practical method for the synthesis of 1,2,4-triazolo[5,1- b ]quinazolin-9(3 H)-ones has been developed via the copper-catalyzed domino reactions of readily available substituted N ′-acetyl-2-bromobenzohydrazides with cyanamide. The protocol uses inexpensive CuI as the catalyst, and no other ligand or additive was required. The target products were prepared in good to excellent yields with tolerance of various functional groups.

Nickel-Catalyzed C-Alkylation of Nitroalkanes with Unactivated Alkyl Iodides

Enabled by nickel catalysis, a mild and general catalytic method for C-alkylation of nitroalkanes with unactivated alkyl iodides is described. Compatible with primary, secondary, and tertiary alkyl iodides; and tolerant of a wide range of functional groups, this method allows rapid access to diverse nitroalkanes.