32937-55-6

Basic information

• Product Name: 2',5'-DIBROMOACETOPHENONE
• Synonyms: 2',5'-DIBROMOACETOPHENONE;1-(2,5-dibromophenyl)ethanone;Ethanone, 1-(2,5-dibromophenyl)-
• CAS NO: 32937-55-6
• Molecular Formula: C₈H₆Br₂O
• Molecular Weight: 277.94
• Product Categories: Aromatic Acetophenones & Derivatives (substituted);Adehydes, Acetals & Ketones;Bromine Compounds
• Mol File: 32937-55-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2',5'-DIBROMOACETOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2',5'-DIBROMOACETOPHENONE(32937-55-6)
• EPA Substance Registry System: 2',5'-DIBROMOACETOPHENONE(32937-55-6)

Safety Data

• Hazardous Substances Data: 32937-55-6(Hazardous Substances Data)

Usage

General Description

2',5'-Dibromoacetophenone is a chemical compound with the molecular formula C8H6Br2O. It is a yellow crystalline solid commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds. 2',5'-Dibromoacetophenone is also employed as a reagent in organic synthesis, particularly in the preparation of complex molecules. Additionally, it has been studied for its potential as an antibacterial agent and for its anti-inflammatory properties. 2',5'-DIBROMOACETOPHENONE is considered to be moderately toxic and should be handled with care in a laboratory setting.

Upstream product

• 59615-13-3 2,5-Dibromobenzoic acid chloride 
• 676-58-4 methylmagnesium chloride 
• 75-16-1 methylmagnesium bromide 
• 98-86-2 acetophenone 
• 610-71-9 2,5-dibromobenzoic acid 
• 106-37-6 1.4-dibromobenzene 
• 75-36-5 acetyl chloride 

Downstream Products

• 203314-28-7 2-(2,5-dibromophenyl)-acetic acid 
• 1374227-74-3 N'-(2-acetyl-4-bromophenyl)-N'-phenylbenzohydrazide 
• 66109-51-1 2-bromo-1-(2,5-dibromophenyl)ethanone 
• 1131453-86-5 6-bromo-2-(2',5'-dibromophenyl)-4-methylquinoline 
• 32917-57-0 2,5-dibromostyrene 
• 128293-94-7 4-(2,5-Dibromo-phenyl)-2-(4-nitro-phenyl)-2,5-dihydro-[1,2,3]thiadiazole 1-oxide 
• 112446-48-7 1-[1-(5-Bromo-2-phenylsulfanyl-phenyl)-ethyl]-4-methyl-piperazine 
• 112446-30-7 4-Bromo-2-(1-chloro-ethyl)-1-phenylsulfanyl-benzene 
• 112446-25-0 1-(5-bromo-2-(phenylthio)phenyl)ethanol 
• 112434-75-0 4-(2,5-Dibromo-phenyl)-5-(2,2-dimethyl-chroman-6-ylazo)-thiazol-2-ylamine 
• 108059-63-8 2-(2-Acetyl-4-bromphenylthio)benzoesaeure-methylester 
• 32917-51-4 1-(2,5-dibromophenyl)ethanol 
• 128293-93-6 2,5-dibromoacetophenone p-nitrophenylhydrazone 
• 112434-79-4 4-(2,5-Dibromo-phenyl)-thiazol-2-ylamine 

Relevant articles and documents

An Improved Process for the Enantioselective Synthesis of HCV NS5A Inhibitor Elbasvir (MK-8742) Chiral Amine Intermediate

Abstract: Large-scale enantioselective synthesis of the chiral amine unit of HCV NS5A inhibitor Elbasvir has been accomplished in six steps, with 55% overall yield. The process includes a highly enantioselective reduction of the NH imine using R-(+)-diphe

Facile synthesis of 1-naphthols through a copper-catalyzed arylation of methyl ketones with o-bromoacetophenones

The coupling reactions of simple methyl ketones with o-bromoacetophenones and subsquential cyclization reactions were realized to produce a range of 1-naphthols. These cascade reactions were initiated by a rare Cu-catalyzed arylation reaction of methyl ketones with aromatic bromides.

Synthesis and characterization of chiral benzylic ether-bridged periodic mesoporous organosilicas

The first synthesis of a chiral periodic mesoporous organosilica (PMO) carrying benzylic ether bridging groups is reported. By hydrolysis and condensation of the new designed chiral organosilica precursor 1,4-bis(triethoxysilyl)-2-(1 -methoxyethyl)benzene