1394240-72-2

Upstream product

• 90536-66-6 4-(methylsulfonyl)phenylacetic acid 
• 75-15-0 carbon disulfide 
• 428508-13-8 2-(4-(methylsulfonyl)phenyl)acetohydrazide 

Downstream Products

• 1394240-79-9 6-(2,5-dichloro-3-thienyl)-3-[4-(methylsulfonyl)benzyl]-7H-[1,2,4]triazolo[3,4-b][1,3,4]-thiadiazine 
• 1394240-78-8 3-{3-[4-(methylsulfonyl)benzyl]-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-6-yl}-1H-isochromen-1-one 
• 1394240-82-4 C₂₅H₁₈Cl₂N₄O₂S₂ 
• 1394240-81-3 2-hydroxy-5-{3-[4-(methylsulfonyl)benzyl]-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-6-yl}benzamide 
• 1394240-77-7 6-(2,4-dichlorophenyl)-3-[4-(methylsulfonyl)benzyl]-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 1394240-76-6 3-[4-(methylsulfonyl)benzyl]-6-(biphenyl-4-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 940060-90-2 3-[4-(methylsulfonyl)benzyl]-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 1394240-75-5 6-(4-methylphenyl)-3-[4-(methylsulfonyl)benzyl]-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 1414883-39-8 4-{[(4-fluorophenyl)methylene]amino}-5-[4-(methylsulfonyl)benzyl]-2,4-dihydro-3H-[1,2,4]-triazole-3-thione 
• 1414883-40-1 4-{[(2-chloro-6-fluorophenyl)methylene]amino}-5-[4-(methylsulfonyl)benzyl]-2,4-dihydro-3H-[1,2,4]-triazole-3-thione 
• 1414883-41-2 C₂₃H₂₀N₄O₂S₂ 
• 1414883-43-4 5-[4-(methylsulfonyl)benzyl]-4-({[4-(methylthio)phenyl]methylene}amino)-2,4-dihydro-3H-[1,2,4]-triazole-3-thione 
• 1414883-45-6 5-[4-(methylsulfonyl)benzyl]-4-({[thiophen-2-yl]methylene}amino)-2,4-dihydro-3H-[1,2,4]-triazole-3-thione 
• 1414883-46-7 4-{[(6-methoxy-2-naphthyl)methylene]amino}-5-[4-(methylsulfonyl)benzyl]-2,4-dihydro-3H-[1,2,4]-triazole-3-thione 

Relevant academic research and scientific papers

Synthesis and biological evaluation of some Schiff bases of 4-amino-5-(4-methylsulfonyl)benzyl-2,4-dihydro-3H-[1,2,4]-triazole-3-thione

The basic nucleus 4-amino-5-[4-(methylsulfonyl)benzyl]-2,4-dihydro-3H-[1,2, 4]-triazole-3-thione was prepared by cyclisation of potassium dithiocarbazinate with hydrazine hydrate using ethanol as solvent under reflux condition. The compound which has been

Facile synthesis, cytotoxic and antimicrobial activity studies of a new group of 6-aryl-3-[4-(methylsulfonyl)benzyl]-7H-[1,2,4]triazolo[3,4-b][1,3,4] thiadiazines

The reaction of 4-(methylsulfonyl)phenylacetohydrazide (3) with carbon disulfide and potassium hydroxide followed by hydrazine hydrate gave 4-amino-5-[4-(methylsulfonyl)benzyl]-4H-[1,2,4]triazole-3-thione (4). The resulting triazole was subjected to cyclo