14901-18-9

Upstream product

• 62-53-3 aniline 
• 82435-83-4 4-Methyl-2-thiazolyl Isothiocyanate 
• 6635-73-0 1-phenyl-2,4-dithiobiuret 
• 78-95-5 chloroacetone 
• 1603-91-4 4-methylthiazol-2-ylamine 
• 103-72-0 phenyl isothiocyanate 

Downstream Products

• 1604812-79-4 C₁₁H₁₁N₃S₂*ClHO₄ 
• 1604812-77-2 C₁₁H₁₁N₃S₂*HNO₃ 
• 1604812-76-1 C₁₁H₁₁N₃S₂*BrH 

Relevant academic research and scientific papers

Polymorphs of 1-(5-methylthiazol-2-yl)-3-phenylthiourea and various anion-assisted assemblies of two positional isomers

Orientations of the phenyl group and the intramolecular hydrogen bond play prime roles in the packing patterns of three conformational polymorphs of an unsymmetrical thiourea derivative, 1-(5-methylthiazol-2-yl)-3-phenylthiourea (PTH1). Self-assembly of e

Formation of Thioamide Derivatives from Reactions of Isothiocyanates with Oxazol-2-amines

4-Substituted oxazol-2-amines react with isothiocyanates to give products having a thioamide function at C5.The reaction is considered to be an electrophilic process in competition with the usual reaction of the amino group with the isothiocyanate.The nature of the isothiocyanate and the type of substituent at C4 affect the amount of the thioamide product formed.Some chemical properties of the thioamides are also investigated.