119550-16-2

Upstream product

• 3173-56-6 benzyl isothiocyanate 
• 28269-82-1 1-phenyl-2-S-benzyl isothiocarbamide 
• 103-85-5 monophenylthiourea 
• 137577-21-0 C₂₂H₂₁N₃OS 
• 78972-46-0 5-Benzyl-1-phenyl-2-thiobiuret 

Downstream Products

• 142427-56-3 2-benzylcarbamoylimino-5,5-bis(ethoxycarbonyl)-3-phenylthiazolidin-4-one 
• 142427-50-7 5-benzylcarbamoylimino-2-ethyl-4-phenyl-1,2,4-thiadiazolidine-3-thione 
• 142427-58-5 2-benzyl-5-(2,3-di-p-tolyl-1-phenylguanidino)-3-oxo-Δ⁴-1,2,4-thiadiazoline 
• 142427-57-4 1-Benzyl-3-[4-phenyl-2-p-tolyl-3-[(Z)-p-tolylimino]-[1,2,4]thiadiazolidin-(5Z)-ylidene]-urea 
• 142427-55-2 2-benzylcarbamoylimino-3,5,5-triphenylthiazolidin-4-one 
• 142427-49-4 5-benzylcarbamoylimino-4-phenyl-3-trichloromethyl-Δ²-1,2,4-thiadiazoline 
• 142427-52-9 3-benzylcarbamoylimino-5-ethoxycarbonylimino-4-phenyl-1,2,4-dithiazolidine 
• 142427-53-0 3-benzoylimino-5-benzylcarbamoylimino-4-phenyl-1,2,4-dithiazolidine 
• 142427-51-8 3-benzylcarbamoylimino-5-(p-nitrophenylimino)-4-phenyl-1,2,4-dithiazolidine 
• 137577-09-4 5-Benzylcarbamoylimino-2-ethyl-4-phenyl-1,2,4-thiadiazolidin-3-one 
• 137577-10-7 5-Benzylcarbamoylimino-2-isopropyl-4-phenyl-1,2,4-thiadiazolidin-3-one 
• 142427-48-3 5-benzylcarbamoylimino-4-phenyl-3-tosyl-Δ²-1,2,4-thiadiazoline 
• 142427-54-1 5-benzylcarbamoylimino-4-phenyl-1,2,4-dithiazolidine-3-thione 

Relevant academic research and scientific papers

Bond-Switch Rearrangement of 3-Oxo-Δ4-1,2,4-thiadiazolin-5-yl Ureas

5-Amino-3-oxo-Δ4-1,2,4-thiadiazolines 5a,b react with isocyanates to yield 1,2,4-thiadiazolidine derivatives 9a-d via bond switching of the corresponding isomers 7.The same type of products 9e-m was obtained by treatment of 5-amino-1,2,3,4-thia

Covalent Adduct Formation in 1,2,4-Thiadiazolo Activated Pyrimidinones

Preparation of 1-(1,2,4-thiadiazol-5-yl)-2(1H)-pyrimidinones is described.The polarization from the thiadiazole ring enhances the ?-electron deficiency of the pyrimidine ring.The latter forms covalently bound adducts with hydroxylic solvent molecules in a regiospecific manner.The adducts are stable, isolable molecules, but on heating in a hydroxylic solvent exchange of the solvent molecule in the adduct may take place.