83806-75-1

Basic information

• Product Name: (4-BROMOPHENYL)(5,7-DIBROMO-1-BENZOFURAN-2-YL)METHANONE
• Synonyms: (4-BROMOPHENYL)(5,7-DIBROMO-1-BENZOFURAN-2-YL)METHANONE;5,7-DIBROMO-2-(4-BROMOBENZOYL)BENZOFURAN
• CAS NO: 83806-75-1
• Molecular Formula: C₁₅H₇Br₃O₂
• Molecular Weight: 458.93
• Mol File: 83806-75-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (4-BROMOPHENYL)(5,7-DIBROMO-1-BENZOFURAN-2-YL)METHANONE(CAS DataBase Reference)
• NIST Chemistry Reference: (4-BROMOPHENYL)(5,7-DIBROMO-1-BENZOFURAN-2-YL)METHANONE(83806-75-1)
• EPA Substance Registry System: (4-BROMOPHENYL)(5,7-DIBROMO-1-BENZOFURAN-2-YL)METHANONE(83806-75-1)

Safety Data

• Hazardous Substances Data: 83806-75-1(Hazardous Substances Data)

Usage

Description

(4-BROMOPHENYL)(5,7-DIBROMO-1-BENZOFURAN-2-YL)METHANONE is a chemical compound belonging to the benzofuran family, characterized by its molecular formula C14H6Br3O2. (4-BROMOPHENYL)(5,7-DIBROMO-1-BENZOFURAN-2-YL)METHANONE features a benzofuran ring with two bromine substitutions at the 5th and 7th positions, a phenyl ring with a single bromine substitution at the 4th position, and a ketone functional group. The unique structural attributes of this compound suggest its potential utility in the realms of pharmaceuticals and agrochemicals, although further research is necessary to explore its full scope of properties and applications.

Uses

Used in Pharmaceutical Industry:
(4-BROMOPHENYL)(5,7-DIBROMO-1-BENZOFURAN-2-YL)METHANONE is used as a compound with potential pharmacological applications due to its unique structural features, including the presence of bromine substitutions and a ketone functional group. These characteristics may contribute to its interaction with biological targets, making it a candidate for the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (4-BROMOPHENYL)(5,7-DIBROMO-1-BENZOFURAN-2-YL)METHANONE may be utilized as a compound with potential biological activities. Its structural components could be harnessed to create novel agrochemicals, such as pesticides or herbicides, that target specific pests or weeds while minimizing harm to the environment and non-target organisms.

Upstream product

• 99-90-1 para-bromoacetophenone 
• 110-86-1 pyridine 
• 110829-99-7 3.5.4'-tribromo-2-hydroxy-trans-chalcone 
• 7726-95-6 bromine 
• 90-59-5 3,5-Dibromosalicylaldehyde 
• 86293-49-4 (E)-1-(4-bromophenyl)-3-(2-hydroxyphenyl)prop-2-en-1-one 
• 99-73-0 para-bromophenacyl bromide 

Downstream Products

• 83806-76-2 (4-Bromo-phenyl)-(5,7-dibromo-benzofuran-2-yl)-methanol 

Relevant articles and documents

Mechanochemical solid-state synthesis of 2-aminothiazoles, quinoxalines and benzoylbenzofurans from ketones by one-pot sequential acid- and base-mediated reactions

α-Chloroketones-obtained by the atom-economical chlorination of ketones with trichloroisocyanuric acid (TCCA) in the presence of p-TSA under ball-milling conditions-were set up for a sequential base-mediated condensation reaction with thiourea/thiosemicarbazides, o-phenylenediamine and salicylaldehyde to afford 2-aminothiazoles, 2-hydrazinylthiazoles, quinoxalines and benzoylbenzofurans, respectively, in respectable yields. The viability of one-pot sequential acid- and base-mediated reactions in the solid state under ball-milling conditions is thus demonstrated.

Reaction of chalcones with NBS, a simple one pot synthesis of 2-aroylbenzo[b]furanes

A simple one pot synthesis of 2-aroylbenzo[b]furanes has been achieved by bromomethoxylation with NBS and subsequent treatment of the appropriately substituted 2-hydroxychalcones with sodium hydroxide.