64382-92-9

Basic information

• Product Name: 2,4-DIBROMO-1-(BROMOMETHYL)BENZENE
• Synonyms: 2,4-DIBROMO-1-(BROMOMETHYL)BENZENE
• CAS NO: 64382-92-9
• Molecular Formula: C₇H₅Br₃
• Molecular Weight: 329
• EINECS: -0
• Mol File: 64382-92-9.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,4-DIBROMO-1-(BROMOMETHYL)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-DIBROMO-1-(BROMOMETHYL)BENZENE(64382-92-9)
• EPA Substance Registry System: 2,4-DIBROMO-1-(BROMOMETHYL)BENZENE(64382-92-9)

Safety Data

• Hazardous Substances Data: 64382-92-9(Hazardous Substances Data)

Usage

General Description

2,4-DIBROMO-1-(BROMOMETHYL)BENZENE is a chemical compound with the molecular formula C7H6Br3. It is a colorless to pale yellow liquid that is insoluble in water but soluble in organic solvents. 2,4-DIBROMO-1-(BROMOMETHYL)BENZENE is primarily used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It is also utilized in the production of insecticides and fungicides. 2,4-DIBROMO-1-(BROMOMETHYL)BENZENE is a brominated aromatic compound that is classified as a potential environmental and human health hazard, with restrictions on its use and handling to minimize exposure.

Upstream product

• 666747-06-4 (2,4-dibromophenyl)methanol 
• 611-00-7 2,4-dibromobenzoic acid 
• 31543-75-6 2,4-dibromotoluene 

Downstream Products

• 666747-06-4 (2,4-dibromophenyl)methanol 
• 92104-02-4 6-bromo-2-phenylbenzofuran 

Relevant articles and documents

Optimization of the chromone scaffold through QSAR and docking studies: Identification of potent inhibitors of ABCG2

The membrane transporter BCRP/ABCG2 has emerged as a privileged biological target for the development of small compounds capable of abolishing multidrug resistance. In this context, the chromone skeleton was found as an excellent scaffold for the design o

Synthetic method 2 and 4 - dibromobenzyl alcohol

The invention provides 2-4 - dibromobenzyl alcohol synthesis method, and the specific steps are as follows: S1, 2, 4 - dibromotoluene is brominated 2 and 4 - dibromobenzyl bromide in a radical initiator. S2 represents 2, 4 - dibromobenzylacetate in acetat

Strategy for Overcoming Full Reversibility of Intermolecular Radical Addition to Aldehydes: Tandem C-H and C-O Bonds Cleaving Cyclization of (Phenoxymethyl)arenes with Carbonyls to Benzofurans

An intermolecular addition of carbon radicals enabled by a cascade radical coupling strategy is developed. It includes an intermolecular alkyl radical addition to a carbonyl group followed by an intramolecular alkoxy radical addition to haloarenes and produces substituted benzofurans in high yields. The radical nature of this reaction is explored by radical trapping experiments and EPR analysis. The mechanism is investigated by KIE experiments and control experiments. This method could provide rapid and practical access to the key intermediate of TAM-16, a safe and potent antibacterial agent for treating tuberculosis, and, therefore, is of great importance for organic synthesis and the pharmaceutical industry.