1018475-06-3

Upstream product

• 1147550-11-5 ammonium thiocyanate 
• 113808-40-5 2-chloro-N-[5-(3-nitrophenyl)-[1,3,4]-thiadiazol-2-yl]-acetamide 
• 833-47-6 5-(3-nitrophenyl)-1,3,4-thiadiazol-2-amine 
• 121-92-6 3-nitrobenzoic acid 

Downstream Products

• 1248828-31-0 5-benzylidene-2-[{5-(3-nitrophenyl)-[1,3,4]-thiadiazol-2-yl}imino]-1,3-thiazolidin-4-one 
• 1248828-41-2 2-[{5-(3-nitrophenyl)-[1,3,4]-thiadiazol-2-yl}imino]-5-(3,4-dimethoxybenzylidene)-1,3-thiazolidin-4-one 

Relevant academic research and scientific papers

Thiadiazole derivatives as potential anticonvulsant agents

A series of thiadiazole derivatives were synthesized with differently substituted benzoic acids which were cyclized to give differently substituted thiazolidin-4-one. Elemental analysis, IR,1HNMR,13C NMR and mass spectral data confir

Synthesis, characterization and antimicrobial activity of new thiadiazole derivatives

A series of thiadiazole derivatives were synthesized with differently substituted benzoic acids which were cyclized to give differently substituted thiazolidin-4-one. Elemental analysis, IR, 1H NMR, 13C NMR and mass spectral data confirmed the

Synthesis of 2-(5-substituted-1,3,4-thiadiazolo-2-ylimino)-4- thiazolidinones under microwave irradiation

Fifteen 2-(5-substituted-1,3,4-thiadiazolo-2-ylimino)-4-thiazolidinones were efficiently synthesized from the reaction of ammonium thiocyanate with 2-chloro-N-(5-substutited-1,3,4-thiadiazolo-2-yl)acetamides under microwave irradiation. The target compoun