83806-46-6

Upstream product

• 99-73-0 para-bromophenacyl bromide 
• 1761-61-1 5-bromosalicyclaldehyde 
• 86293-49-4 (E)-1-(4-bromophenyl)-3-(2-hydroxyphenyl)prop-2-en-1-one 
• 81585-72-0 1-(4-bromo-phenyl)-2-iodo-ethanone 
• 93513-95-2 3-(5-bromo-2-hydroxyphenyl)-1-(4-bromophenyl)prop-2-en-1-one 

Downstream Products

• 1370016-07-1 6-chloro-4'-[5-(2-chloro-5-cyanophenyl)benzofuran-2-carbonyl]biphenyl-3-carbonitrile 
• 1370016-05-9 1-{3-[2-(2'-acetylbiphenyl-4-carbonyl)benzofuran-5-yl]phenyl}ethanone 
• 1370016-03-7 (4'-vinylbiphenyl-4-yl)[5-(4-vinylphenyl)benzofuran-2-yl]methanone 
• 1370016-01-5 (3'-methanesulfonylbiphenyl-4-yl)[5-(3-methanesulfonylphenyl)benzofuran-2-yl]methanone 
• 1370015-99-8 (3'-nitrobiphenyl-4-yl)[5-(3-nitrophenyl)benzofuran-2-yl]methanone 
• 1370015-97-6 (2'-fluorobiphenyl-4-yl)[5-(2-fluorophenyl)benzofuran-2-yl]methanone 
• 1370015-95-4 (2'-ethoxybiphenyl-4-yl)[5-(2-ethoxyphenyl)benzofuran-2-yl]methanone 
• 1370015-93-2 (4'-ethylbiphenyl-4-yl)[5-(4-ethylphenyl)benzofuran-2-yl]methanone 
• 1370015-91-0 [1,1'-biphenyl]-4-yl(5-phenylbenzofuran-2-yl)methanone 
• 1370016-39-9 (3'-nitrobiphenyl-4-yl)[5-(3-nitrophenyl)benzofuran-2-yl]methanol 
• 1370016-37-7 (2'-fluorobiphenyl-4-yl)[5-(2-fluorophenyl)benzofuran-2-yl]methanol 
• 1370016-35-5 (4'-ethylbiphenyl-4-yl)-[5-(4-ethylphenyl)benzofuran-2-yl]methanol 
• 1370016-33-3 biphenyl-4-yl(5-phenylbenzofuran-2-yl)methanol 
• 1370016-31-1 1-(2'-ethoxybiphenyl-4-yl)-1-[5-(2-ethoxyphenyl)benzofuran-2-yl]-2-phenylethanol 

Relevant academic research and scientific papers

Synthesis, characterization, and antimicrobial activity of new benzofuran derivatives

A novel series of (5-substituted-1-benzofuran-2-yl)(2,4-substituted phenyl)methanones (4a–4i) have been prepared by the Knoevenagel condensation of (5-substituted-1-benzofuran-2-yl)(2,4-substituted phenyl)methanone (3a–3i) with Meldrum’s acid. The structu

Synthesis and antitubercular activity of 4-thiazolidinone derivatives incorporating benzofuran moiety

5-Bromo-1-benzofuran-2-yl(substituted phenyl) methanones (2a-e) were prepared by the reaction of 2-bromo-1-(phenyl) ethanones and 5-bromosalicylaldehyde in dimethylformamide in the presence of anhydrous potassium carbonate to maintain basic condition. Con

5-phenyl-1-benzofuran-2-yl derivatives: Synthesis, antimicrobial, and antioxidant activity

Previously unknown biphenyl containing 5-phenyl-1-benzofuran-2-yl derivatives; methanones (2a-i), tertiary alcohols (3a-l), and carbinols (4a-f) were synthesized and evaluated for their antimicrobial and antioxidant activities to study the effect of funct

Reaction products of 5-bromobenzofuran-2-yl-aryl methanone and their antimicrobial activities

5-Bromobenzofuran-2-yl-aryl methanones (2a-e) were obtained by the reaction of 5-bromosalicylaldehyde 1 with 2-bromo-1-(aryl) ethanones. The condensation of compounds (2a-e) with hydroxylamine hydrochloride, thiosemicarbazide and aromatic amine such as an

DMAP-catalyzed cascade reaction: One-pot synthesis of benzofurans in water

A series of benzofurans were efficiently synthesized in good to excellent yields using 4-dimethylaminopyridine (DMAP) catalyzed cascade reaction between salicylaldehydes and halogenated ketones in water at 80 °C opened atmosphere.

Microwave-mediated solvent free Rap-Stoermer reaction for efficient synthesis of benzofurans

The Rap-Stoermer reaction of salicylaldehydes with diverse phenacyl bromide and phenacyl iodides proceeded cleanly to afford various functionalized benzofurans in excellent yields under base-mediated solvent free microwave irradiation conditions.

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.