92973-13-2

Upstream product

• 92973-24-5 5-(2-(trifluoromethyl)phenyl)furan-2-carboxylic acid 
• 773874-52-5 5-[2-(trifluoromethyl)phenyl]furan-2-carboxylic acid methyl ester 
• 2527-99-3 methyl 5-bromo-2-furoate 
• 1423-27-4 2-(trifluoromethyl)phenylboronic acid 

Downstream Products

• 900136-68-7 2-(2-furyl)-5-[5-(2-trifluoromethylphenyl)furan-2-yl]-1,3,4-oxadiazole 
• 92972-82-2 {5-[5-(2-Trifluoromethyl-phenyl)-furan-2-yl]-tetrazol-1-yl}-acetic acid 
• 92973-10-9 {5-[5-(2-Trifluoromethyl-phenyl)-furan-2-yl]-tetrazol-1-yl}-acetic acid ethyl ester 
• 92972-99-1 {[1-Chloro-1-[5-(2-trifluoromethyl-phenyl)-furan-2-yl]-meth-(Z)-ylidene]-amino}-acetic acid ethyl ester 
• 92973-20-1 {[5-(2-Trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}-acetic acid ethyl ester 

Relevant academic research and scientific papers

Synthesis and SAR of 5-aryl-furan-2-carboxamide derivatives as potent urotensin-II receptor antagonists

The synthesis and biological evaluation as potential urotensin-II receptor antagonists of a series of 5-arylfuran-2-carboxamide derivatives 1, bearing a 4-(3-chloro-4-(piperidin-4-yloxy)benzyl)piperazin-1-yl group, are described. The results of a systemat

Synthesis of heterocycles from arylation products of unsaturated compounds: XVIII. 5-Arylfuran-2-carboxylic acids and their application in the synthesis of 1,2,4-thiadiazole, 1,3,4-oxadiazole, and [1,2,4]triazolo[3,4-b][1,3,4] thiadiazole derivatives

Arylation of furan-2-carboxylic acid or its methyl ester with arenediazonium chlorides in the presence of copper(II) chloride gave the corresponding 5-arylfuran-2-carboxylic acids or methyl 5-arylfuran-2- carboxylates. 5-Arylfuran-2-carbonyl chlorides rea