77303-41-4

Upstream product

• 5338-82-9 4-phenyl-5-phenylimino-[1,2,4]dithiazolidin-3-one 
• 103-71-9 phenyl isocyanate 
• 55211-01-3 4-Phenyl-3,5-bisphenylimino-1,2,4-dithiazolidin 
• 1986-08-9 S-chloro-N-phenylisothiocarbamoyl chloride 
• 102-07-8 bis(diphenyl)urea 
• 103-72-0 phenyl isothiocyanate 
• 63891-95-2 S-benzyl-N,N'-diphenyl-isothiourea 
• 91732-62-6 1,3,5-trisubstitutedphenyl-2S-benzylisobiuret 

Downstream Products

• 139119-37-2 [3-(2,6-Di-tert-butyl-phenoxy)-4-phenyl-4H-[1,2,4]thiadiazol-(5E)-ylidene]-phenyl-amine 
• 139119-36-1 [3-(2,6-Dimethyl-phenoxy)-4-phenyl-4H-[1,2,4]thiadiazol-(5E)-ylidene]-phenyl-amine 
• 139119-34-9 Phenyl-[4-phenyl-3-p-tolyloxy-4H-[1,2,4]thiadiazol-(5E)-ylidene]-amine 
• 139119-33-8 [3-(4-Chloro-phenoxy)-4-phenyl-4H-[1,2,4]thiadiazol-(5E)-ylidene]-phenyl-amine 
• 139119-35-0 [3-(4-Methoxy-phenoxy)-4-phenyl-4H-[1,2,4]thiadiazol-(5E)-ylidene]-phenyl-amine 
• 106696-31-5 1,3,5-Triphenyl-thiobiuret 
• 103-71-9 phenyl isocyanate 
• 622-16-2 1,3-Diphenylcarbodiimide 
• 139119-38-3 Phenyl-[4-phenyl-3-trichloromethyl-4H-[1,2,4]thiadiazol-(5E)-ylidene]-amine 
• 4695-01-6 3,5,5-triphenyl-2-phenylimino-thiazolidin-4-one 
• 4694-99-9 3,5-diphenyl-2-phenylimino-thiazolidin-4-one 
• 18334-60-6 4-phenyl-5-phenylimino-3-thio-1,2,4-thiadiazolidine 
• 4695-23-2 5,5-dimethyl-3-phenyl-2-phenylimino-thiazolidin-4-one 

Relevant academic research and scientific papers

Cycloaddition Elimination Reactions of 4-Aryl-5-arylimino-1,2,4-dithiazolidin-3-ones (Mustard Oil Oxides)

4-Aryl-5-arylimino-1,2,4-dithiazolidin-3-ones (1) react with isocyanates, isothiocyanates, and cyanic acid esters by exchange of the COS-part from 1 affording thiadiazole and dithiazole derivatives 4, 5, 6, or 12.The reaction products are able to give fur

Synthesis of 4-Aryl-5-arylimino-3-oxo-2-phenyl-1,2,4-thiadiazolidines

4-Aryl-5-arylimino-3-oxo-2-phenyl-1,2,4-thiadiazolidines (IV) have been prepared by the oxidation of the corresponding 1,3-diaryl-2-S-benzyl-5-phenylisothiobiurets (III) with bromine in chloroform.A plausible mechanism for the reaction has been suggested.

3-Oxo-5-Phenylimino-1,2,4-thiadiazolidine and Its Some Aryl Analogues

Certain 3-oxo-2-unsubstituted/aryl substituted-4-unsubstituted/aryl substituted-5-phenylimino-1,2,4-thiadiazolidines involving interaction of S-chloro-N-phenyl isothiocarbamoyl chloride and parent and mono- and di-aryl carbamides have been prepared.Their structural assignments have been made on the basis of certain chemical transformations and IR spectral analysis.