347190-82-3

Upstream product

• 251577-90-9 2,5-bis(2-methyl-4-nitrophenyl)furan 

Downstream Products

• 347190-88-9 2,5-bis(2-methyl-4-N,N'-di-BOCguanidinophenyl)furan 
• 1189132-48-6 N,N'-[4,4'-(furan-2,5-diyl)bis(3-methyl-4,1-phenylene)]bis[1-(4-chlorophenylsulfonyl)-1H-indole-3-sulfonamide] 
• 1189132-44-2 N,N'-[4,4'-(furan-2,5-diyl)bis(3-methyl-4,1-phenylene)]bis[1-(4-bromophenylsulfonyl)-1H-indole-3-sulfonamide] 
• 1189132-40-8 N,N'-[4,4'-(furan-2,5-diyl)bis(3-methyl-4,1-phenylene)]bis[1-(4-methoxyphenylsulfonyl)-1H-indole-3-sulfonamide] 
• 1189132-46-4 N,N'-[4,4'-(furan-2,5-diyl)bis(3-methyl-4,1-phenylene)]bis[1-(4-methylphenylsulfonyl)-1H-indole-3-sulfonamide] 
• 1189132-42-0 N,N'-[4,4'-(furan-2,5-diyl)bis(3-methyl-4,1-phenylene)]bis[1-(phenylsulfonyl)-1H-indole-3-sulfonamide] 

Relevant academic research and scientific papers

Novel furanylarylene arylsulfonylindolesulfonamides: Synthesis and their antibacterial evaluation

An array of furanylarylene arylsulfonylindolesulfonamides was synthesized through multi-step synthetic protocols involving bromination, stannylation, Stille cross coupling, reduction, arylsulfonylation, chlorosulfonylation, and condensation reactions. As

Compounds, methods and compositions useful for the treatment of bovine viral diarrhea virus (BVDV) infection and hepatitis C virus (HCV) infection

The present invention relates to novel compounds and methods that are useful in treating members of the Flaviviridae family of viruses. Compounds of the present invention will have a structure according to Formulas (I)-(VI) as recited throughout the appli

Diguanidino and "reversed" diamidino 2,5-diarylfurans as antimicrobial agents

Dicationic 2,5-bis(4-guanidinophenyl)furans 5a-5f, 2,5-bis[4- (arylimino)aminophenyl]furans 6a-6b and 6e-6k, and 2,5-bis[4-(alkylimino)aminophenyl]furans 6c-6d have been synthesized starting from 2,5-bis[tri-n-butylstannyl]furan. Thermal melting studies w