114382-18-2

Upstream product

• 108106-08-7 N-(3-phenyl-5-thioxo-1,5-dihydro-[1,2,4]triazol-4-yl)-formamide 
• 64-18-6 formic acid 
• 22706-11-2 4-amino-3-phenyl-1H-1,2,4-triazole-5(4H)-thione 

Downstream Products

• 1627096-47-2 3-phenyl-5-(p-tolylthio)-1H-1,2,4-triazole 
• 1627096-48-3 3-phenyl-5-(phenylthio)-1H-1,2,4-triazole 
• 1627096-49-4 3-phenyl-5-(o-tolylthio)-1H-1,2,4-triazole 
• 1627096-50-7 3-phenyl-5-{[4-(trifluoromethyl)phenyl]thio}-1H-1,2,4-triazole 
• 1627096-51-8 ethyl 4-[(3-phenyl-1H-1,2,4-triazol-5-yl)thio]benzoate 
• 1627096-52-9 5-[(4-methoxyphenyl)thio]-3-phenyl-1H-1,2,4-triazole 
• 1627096-48-3 C₁₄H₁₁N₃S 
• 1627096-52-9 C₁₅H₁₃N₃OS 
• 1627096-53-0 3-{[4-(phenoxymethyl)phenyl]thio}-5-phenyl-1H-1,2,4-triazole 
• 7747-19-5 3-(methylthio)-5-phenyl-1H-1,2,4-triazole 
• 141922-23-8 3-(ethylthio)-5-phenyl-1H-1,2,4-triazole 
• 923160-24-1 3-(isopropylthio)-5-phenyl-1H-1,2,4-triazole 
• 1627096-54-1 3-(tert-butylthio)-5-phenyl-1H-1,2,4-triazole 
• 110960-77-5 5-phenyl-3-(vinylthio)-1H-1,2,4-triazole 

Relevant academic research and scientific papers

STUDIES ON 4-AMINO-5-ARYL-1,2,4-TRIAZOLE-3-THIONES

4-Amino-5-aryl-1,2,4-triazole-3-thiones 1 react with phenacylbromide at room temperature to give 2, which could be converted to 3 on reflux. Treatment of 1 with chloroacetonitrile and potassium hydroxide in equimolar ratio and in excess yielded 4 and 6, r