79491-00-2

Upstream product

• 622-52-6 p-methylphenylthiourea 
• 592-82-5 butyl isothiocyanate 
• 622-59-3 1-isothiocyanato-4-methylbenzene 
• 79490-96-3 3-p-tolylimino-5-butylimino-1,2,4-dithiazolidine 
• 79490-96-3 [5-[(Z)-Butylimino]-[1,2,4]dithiazolidin-(3E)-ylidene]-p-tolyl-amine 
• 94686-01-8 2-benzyl-1-butyl-3-(p-tolyl-thiocarbamoyl)-isothiourea 

Downstream Products

• 79490-96-3 3-p-tolylimino-5-butylimino-1,2,4-dithiazolidine 

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

Reaction of Isothiocyanates with Thiourea--a Correction

The condensation products of isothiocyanates with thiourea reported to be S-(N-substituted thiocarbamoyl)isothioureas are in fact 1-substituted 2,4-dithiobiurets and not the former.The condensation of isothiocyanates with 1-substituted thioureas also is f