30544-34-4

Usage

Uses

Used in Pharmaceutical Synthesis:
2,3-Dibromofuran is used as a key intermediate for the synthesis of pharmaceuticals, contributing to the development of new drugs due to its reactivity in chemical reactions.
Used in Agrochemical Production:
In the agrochemical industry, 2,3-Dibromofuran serves as a crucial component in the creation of various agrochemicals, playing a significant role in enhancing agricultural productivity and pest control.
Used as a Reagent in Organic Synthesis:
2,3-Dibromofuran is utilized as a reagent in organic synthesis, facilitating specific chemical reactions that are essential for the production of a range of organic compounds.
Used in Specialty Chemicals Production:
As a building block, 2,3-Dibromofuran is employed in the manufacturing process of specialty chemicals, which are used across different industries for their unique properties and applications.

InChI:InChI=1/C4H2Br2O/c5-3-1-2-7-4(3)6/h1-2H

Upstream product

• 2434-03-9 4,5-dibromo-2-furoic acid 
• 89284-17-3 2,3,4,5-tetrabromo-tetrahydro-furan-2-carboxylic acid 
• 98-01-1 furfural 

Downstream Products

• 14757-78-9 3-bromofurfural 
• 2433-85-4 4,5-dibromo-2-furancarboxaldehyde 
• 1266329-44-5 3-bromo-2-(phenylethynyl)furan 
• 1312996-86-3 5-(3-bromo-2-furyl)-2-methoxyphenol 
• 1312996-84-1 3-bromo-2(4′-methoxyphenyl)furan 
• 1312996-81-8 3-bromo-2-(3,4,5-trimethoxyphenyl)furan 
• 171617-77-9 (Ss)-3-bromo-2-(p-tolylsulfinyl)-furane 
• 49777-66-4 1-(3-dihydroxyboranyl-furan-2-yl)-ethanone 
• 1332869-81-4 2,3-di(p-tolyl)furan 
• 83457-06-1 3-bromo-2-methylfuran 
• 4828-13-1 4,5-dibromo-2-(diethoxymethyl)-furan 

Relevant academic research and scientific papers

Synthesis of substituted bis(heteroaryl)maleimides

Substituted bis(fur-2-yl), bis(fur-3-yl) and bis(thien-2-yl) maleimides with potential antidiabetic properties are described. Their synthesis involves, as a key step, a Suzuki cross-coupling between various boron derivatives and the diiodomaleimides. Therefore, a wide range of substituted symmetric and non-symmetric maleimide derivatives can be prepared.

The preparation of 2,3,5-tri- and 2,3-disubstituted furans by regioselective palladium(0)-catalyzed coupling reactions: Application to the syntheses of rosefuran and the F5 furan fatty acid

The 5-acceptor-substituted 2,3-dibromofurans 1 and 2 underwent a regioselective Pd0-catalyzed coupling reaction at the C-2 carbon atom. With alkynes the corresponding 2-alkynylfurans 4 and 5 were accessible (49-97% yield) Alkyl-, aryl-, and alk

Two Syntheses of Manoalide via Heteroatom-Assisted Alkyne Carbometallation

Two approaches to the sesterterpenoid phospholipase A2 inhibitors seco-manoalide (3) and manoalide (1) are described based on carbometallation of propargylic alcohols to generate the functionalised C6-C7 trisubstituted alkene.Both syntheses also deploy the photooxidation of a furan in order to generate a 4-substituted 5-hydroxy-2(5H)-furanone moiety.