57633-36-0

Upstream product

• 93881-77-7 2-allyl-1-(4-chloro-phenyl)-3-(p-tolyl-thiocarbamoyl)-isothiourea 
• 97379-79-8 C₁₅H₁₂ClN₃S₂*HI 
• 57633-28-0 2-allyl-1-[(4-chloro-phenyl)-thiocarbamoyl]-3-p-tolyl-isothiourea 

Downstream Products

• 83772-93-4 N-(4-Chloro-phenyl)-N'-p-tolyl-4H-[1,2,4]triazole-3,5-diamine 
• 57633-42-8 1-p-Tolyl-5-<4-chlor-phenyl>-2.4-dithiobiuret 

Relevant academic research and scientific papers

A One-Step Synthesis of 1,5-Disubstituted 2,4-Dithiobiurets and Their Oxidation to 3,5-Di(substitutedimino)-1,2,4-dithiazolidines

In presence of alkali, 1-substituted thioureas condense with isothiocyanates forming 1,5-disubstituted 2,4-dithiobiurets (2).The structure of the products has been confirmed by chemical as well as spectral studies.Oxidation of 2 yields 3,5-di(substitutedi