70208-17-2

Upstream product

• 90959-38-9 C₂₀H₁₈ClN₃O₂S 
• 104-88-1 4-chlorobenzaldehyde 
• 5351-69-9 4-Phenyl-3-thiosemicarbazide 
• 90959-29-8 C₁₄H₁₂Cl₂N₂O₂S 
• 62-53-3 aniline 

Relevant academic research and scientific papers

Synthesis of 1,2,4-Triazoles via Oxidative Heterocyclization: Selective C-N Bond over C-S Bond Formation

The higher propensity of C-N over C-S bond forming ability was demonstrated, through formal C-H functionalization during the construction of 4,5-disubstituted 1,2,4-triazole-3-thiones from arylidenearylthiosemicarbazides catalyzed by Cu(II). However, ster

Base-induced Dehydrosulfinatocyclization of N-Alkyl-N-phenylsulfonyl-N''-arylbenzamidrazones to 3,4-Diaryl-4H-1,2,4-triazoles

3,4-Diaryl-4H-1,2,4-triazoles were obtained in good to comparable yields by the reaction of N-alkyl-N-phenylsulfonyl-N''-arylbenzamidrazones with sodium hydride.The reaction probably proceeds via the elimination of benzenesulfinic acid and the oxidative cyclization of N-alkylidene-N''-arylbenzamidrazones generated by the base-catalyzed isomerization of azo intermediates.