885681-96-9

Basic information

• Product Name: 4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene
• Synonyms: 4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene;4-Bromo-2-iodobenzyl bromide 97%;4-Bromo-2-iodobenzylbromide97%;4-Bromo-2-Iodobenzyl Bromide;4-Bromo-1-(bromomethyl)-2-iodobenzene
• CAS NO: 885681-96-9
• Molecular Formula: C₇H₅Br₂I
• Molecular Weight: 375.82707
• Mol File: 885681-96-9.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene(885681-96-9)
• EPA Substance Registry System: 4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene(885681-96-9)

Safety Data

• Hazardous Substances Data: 885681-96-9(Hazardous Substances Data)

Usage

General Description

The chemical compound "4-Bromo-1-(bromomethyl)-2-iodobenzene, alpha,4-Dibromo-2-iodotoluene" is a combination of two different chemicals: 4-bromo-1-(bromomethyl)-2-iodobenzene and alpha,4-Dibromo-2-iodotoluene. Both of these chemicals belong to the class of aromatic compounds and are characterized by the presence of bromine and iodine atoms. They are used in various industrial applications, including the production of pharmaceuticals, dyes, and other organic substances. These chemicals are also used in research and development laboratories for their unique properties and reactivity. However, due to their potentially hazardous nature, they require careful handling and storage to prevent any adverse effects on human health and the environment.

Upstream product

• 1133123-02-0 4-bromo-2- iodobenzoic acid 
• 1261438-69-0 (4-bromo-2-iodophenyl)methanol 
• 39478-78-9 5-bromo-2-methylaniline 
• 106-38-7 para-bromotoluene 
• 260558-15-4 4-bromo-2-iodo-1-methylbenzene 

Downstream Products

• 1279129-86-0 (Z)-1,2-bis(4-bromo-2-iodophenyl)ethene 
• 1261470-87-4 5-bromo-1-iodo-2-benzaldehyde 
• 1279129-88-2 3,7-dibromo-5-(2,4,6-tri-tert-butylphenyl)dibenzo[b,f]borepin 
• 1279129-91-7 3,7-di(thiophen-2-yl)-5-(2,4,6-tri-tert-butylphenyl)dibenzo[b,f]borepin 
• 1279129-93-9 3,7-bis(4-methoxyphenyl)-5-(2,4,6-tri-tert-butylphenyl)dibenzo[b,f]borepin 
• 1279129-94-0 3,7-bis(phenylethynyl)-5-(2,4,6-tri-tert-butylphenyl)dibenzo[b,f]borepin 
• 1279129-97-3 5-(2,4,6-tri-tert-butylphenyl)dibenzo[b,f]borepin-3,7-dicarboxylic acid 

Relevant articles and documents

Practical method for preparation of 2-[18F]fluoro-4-boronophenylalanine

2 - Containing radioactive isotopes18 F] Fluoro -4 - boronylphenylalanine18 F [FBPA] A process for the preparation of the same. [18 F-FBPA is an efficient target compound by suggesting a precursor and reaction conditions w

CuSO4-Catalyzed Tandem C(sp3)-H Insertion Cyclization of Toluenes with Isonitriles to Form Indoles

A CuSO4-catalyzed tandem benzylic C-H insertion cyclization of toluene derivatives and isonitriles is described. The naturally abundant salt CuSO4 serves as a low-cost ligand-free redox catalyst. This reaction provides a practical mo

CuSO4-Catalyzed dual annulation to synthesize O, S or N-containing tetracyclic heteroacenes

In this work, CuSO4 is utilized as a practical redox catalyst for tandem dual annulation in the synthesis of indole-fused tetracyclic heteroacenes, which are important skeletons in both medicinal chemistry and materials chemistry. The preparation of such skeletons in a convenient and efficient manner is in high demand. This method realizes the modular synthesis of benzofuro-, benzothieno-, and indoloindoles from abundant feedstocks such as 2-halobenzyl halides and nitrile derivatives in up to 99% yields, providing a rapid access to diverse indole-fused heteroacenes with biological or optoelectronic properties.