132395-52-9

Upstream product

• 75-15-0 carbon disulfide 
• 82117-98-4 5-Amino-3-methylthio-1-phenyl-1H-1,2,4-triazole 
• 74-88-4 methyl iodide 

Downstream Products

• 140473-46-7 1-(1-Hydroxymethyl-propyl)-2-methyl-3-(5-methylsulfanyl-2-phenyl-2H-[1,2,4]triazol-3-yl)-isothiourea 
• 140473-45-6 1-(2-Hydroxy-propyl)-2-methyl-3-(5-methylsulfanyl-2-phenyl-2H-[1,2,4]triazol-3-yl)-isothiourea 
• 140473-66-1 C₂₅H₃₀N₁₀S₄ 
• 140473-72-9 1-acetyl-2-<(3-methylthio-1-phenyl-1H-1,2,4-triazol-5-yl)imino>oxazolidine 
• 140473-73-0 1-acetyl-2-<(3-methylthio-1-phenyl-1H-1,2,4-triazol-5-yl)imino>thiazolidine 
• 140473-44-5 1-(3-Hydroxy-propyl)-2-methyl-3-(5-methylsulfanyl-2-phenyl-2H-[1,2,4]triazol-3-yl)-isothiourea 
• 140473-65-0 C₂₄H₂₈N₁₀S₄ 
• 140473-43-4 1-(2-Hydroxy-ethyl)-2-methyl-3-(5-methylsulfanyl-2-phenyl-2H-[1,2,4]triazol-3-yl)-isothiourea 
• 140473-64-9 2-<(3-methylthio-1-phenyl-1H-1,2,4-triazole-5-yl)imino>thiazolidine 

Relevant academic research and scientific papers

On Triazoles. XXII. Synthesis of Dialkyl (3-Q-1,2,4-Triazol-5-yl)iminodithiocarbonates

Isomeric dialkyl and diaralkyliminodithiocarbonates 4a-c (R not equal H) were synthesised and their spectral data compared.The uv, cmr and ms rules elaborated helped to prove the tautomeric structure of the non-substituted derivatives 4 (R = H).In case of dimethyl (3-methylthio-1,2,4-triazol-5-yl)iminodithiocarbonate this is the first time ever crystalline triazole desmotropes 4a/17 and 4b/17 could be isolated.The sodium salts of 4 (R = H) could be further alkylated and aralkylated to yield the corresponding 4 (R = alkyl and aralkyl) type derivatives.Providing the above reaction in the presence of carbon disulfide the dithiocarbomethoxy derivative 7 was obtained.