43045-25-6

Upstream product

• 10531-41-6 2-Bromoacetylthiophene 
• 1124-15-8 3,5-dimethyl-1H-pyrazole-1-carbothioamide 

Downstream Products

• 119701-67-6 2,3-dihydro-2-imino-3-phenyl-5-thienoyl-1,3,4-thiadiazole 
• 119701-68-7 (5-Imino-4-p-tolyl-4,5-dihydro-[1,3,4]thiadiazol-2-yl)-thiophen-2-yl-methanone 
• 119701-69-8 [5-Imino-4-(4-methoxy-phenyl)-4,5-dihydro-[1,3,4]thiadiazol-2-yl]-thiophen-2-yl-methanone 
• 119701-70-1 [4-(4-Chloro-phenyl)-5-imino-4,5-dihydro-[1,3,4]thiadiazol-2-yl]-thiophen-2-yl-methanone 
• 119701-71-2 [5-Imino-4-(4-nitro-phenyl)-4,5-dihydro-[1,3,4]thiadiazol-2-yl]-thiophen-2-yl-methanone 
• 1258795-43-5 (1-(4-(thiophen-2-yl)thiazol-2-yl)-1H-1,2,3-triazol-4-yl)methyl (E)-cinnamate 
• 1258795-39-9 4-phenyl-1-(4-(thiophen-2-yl)thiazol-2-yl)-1H-1,2,3-triazole 
• 119701-86-9 C₁₃H₇N₅O₄S₂ 
• 119701-84-7 C₁₄H₁₀N₄O₃S₂ 
• 119701-85-8 C₁₃H₇ClN₄O₂S₂ 
• 119701-83-6 C₁₄H₁₀N₄O₂S₂ 
• 119701-82-5 C₁₃H₈N₄O₂S₂ 

Relevant academic research and scientific papers

Unexpected Formation of α-Thiocyanatoketones in Hantzsch Thiazole Synthesis

The reaction of 3,5-dimethylpyrazole-1-thiocarboxamide (3) with α-haloketones (4) yields the corresponding α-thiocyanatoketones (5) or pyrazoles (1) depending upon nature of the halogen.Many such pyrazole derivatives have erroneously been described as thiazolotriazepines in literature.