82386-91-2

Basic information

• Product Name: 2-(bromomethyl)-4-chloro-1-iodobenzene
• Synonyms: 2-(bromomethyl)-4-chloro-1-iodobenzene
• CAS NO: 82386-91-2
• Molecular Weight: 331.378
• Mol File: 82386-91-2.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2-(bromomethyl)-4-chloro-1-iodobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(bromomethyl)-4-chloro-1-iodobenzene(82386-91-2)
• EPA Substance Registry System: 2-(bromomethyl)-4-chloro-1-iodobenzene(82386-91-2)

Safety Data

• Hazardous Substances Data: 82386-91-2(Hazardous Substances Data)

Usage

General Description

2-(bromomethyl)-4-chloro-1-iodobenzene is a chemical compound that contains a benzene ring with a bromomethyl group attached at the 2 position, a chlorine atom at the 4 position, and an iodine atom at the 1 position. It is a derivative of benzene and is used as a building block in the synthesis of various organic compounds. 2-(bromomethyl)-4-chloro-1-iodobenzene may have applications in pharmaceuticals, agrochemicals, and materials science due to its potential for introducing functional groups and structural diversity into organic molecules. It is important to handle this chemical with caution, as it may be hazardous and should be used in a controlled and regulated manner.

Upstream product

• 23399-70-4 4-chloro-1-iodo-2-methylbenzene 
• 13421-00-6 5-chloro-2-iodo-benzoic acid 
• 15396-37-9 2-iodoyl-3,5-dichlorobenzoic acid 
• 82386-90-1 5-chloro-2-iodobenzyl alcohol 

Downstream Products

• 1178576-95-8 2-benzenesulfonylmethyl-4-chloro-1-iodo-benzene 
• 251353-79-4 3-[2-(5-chloro-2-iodo-phenyl)-ethyl]-pyridine-2-carboxylic acid methyl-phenyl-amide 
• 31251-41-9 8-chloro-5,6-dihydro-11H-Benzo[5,6]cyclohepta[1,2-b]pyridin-11-one 
• 251353-78-3 3-[2-(5-chloro-2-iodo-phenyl)-ethyl]-pyridine-2-carboxylic acid phenylamide 
• 82386-94-5 2-(Chloro-2-iodobenzylthio)phenol 

Relevant articles and documents

COMPOUNDS HAVING BOTH EFFECTS OF BET BROMODOMAIN PROTEIN INHIBITION AND PD-L1 GENE REGULATION

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tBuOK-Promoted Cyclization of Imines with Aryl Halides

A transition-metal-free indole synthesis using radical coupling of 2-halotoluenes and imines via the later-stage C-N bond construction was reported for the first time. It includes an aminyl radical generation by C-H cleaving addition of 2-halotoluenes to imines via the carbanion radical relay and an intramolecular coupling of aryl halides with aminyl radicals. One standard condition can be used for all halides including F, Cl, Br, and I. No extra oxidant or transition metal is required.

Access to chiral tetrahydrofluorenes through a palladium-catalyzed enantioselective tandem intramolecular Heck/Tsuji-Trost reaction

A palladium-catalyzed enantioselective coupling of 2,5-cyclohexadienyl-substituted aryl iodides and carbon or heteroatom nucleophiles is described. The reaction proceeded via a tandem asymmetric Heck insertion and Tsuji-Trost allylation, enabling the rapi