77420-76-9

Upstream product

• 77420-51-0 C₁₅H₁₃ClN₂ 
• 77420-61-2 3-methyl-benzoic acid benzylidenehydrazide 
• 13050-47-0 3-methylbenzoyl hydrazine 
• 120-33-2 ethyl 3-methylbenzoate 
• 881-73-2 2-(3-methylbenzoyl)hydrazinecarbothioamide 
• 77420-71-4 N-[1-Phenyl-meth-(E)-ylidene]-N'-[1-thiocyanato-1-m-tolyl-meth-(Z)-ylidene]-hydrazine 
• 76074-47-0 5-(3-methylphenyl)-1,3,4-thiadiazol-2-amine 
• 100-52-7 benzaldehyde 

Downstream Products

• 84304-45-0 6-(4-Chloro-phenyl)-7-phenyl-2-m-tolyl-6,7-dihydro-[1,3,4]thiadiazolo[3,2-a][1,3,5]triazine-5-thione 
• 84304-36-9 6,7-Diphenyl-2-m-tolyl-6,7-dihydro-[1,3,4]thiadiazolo[3,2-a][1,3,5]triazine-5-thione 
• 84304-41-6 6-(2-Chloro-phenyl)-7-phenyl-2-m-tolyl-6,7-dihydro-[1,3,4]thiadiazolo[3,2-a][1,3,5]triazine-5-thione 

Relevant academic research and scientific papers

1,4-Cycloaddition of Isothiocyanates to Azomethines and Fungitoxicity of Resulting 1,3,4-Thiadiazolo-s-triazine-5(6H,7H)-thiones

Several 2,6,7-trisubstituted 1,3,4-thiadiazolo-s-triazine-5(6H,7H)-thiones have been prepared by 1,4-cycloaddition of aryl isothiocynates to 5-aryl(aryloxymethyl-2-benzylidene-amino-1,3,4-thiadiazoles (3a-e).The fungicidal activity of compounds has

Unsaturated Compounds containing Nitrogen. Part 4. Further Reactions of 1-Chloro-2,3-diazabutadienes with S-Nucleophiles

1-Chloro-1,4-diaryl-2,3-diazabutadienes (Ar1CCl=NN=CHAr2), prepared by the reaction of thionyl chloride with aroylhydrazones (Ar1CONHN=CHAr2), react with thiosemicarbazide or thiocarbohydrazide to give 2-arylidenehydrazino-5-aryl-1,3,4-thiadiazoles, and with potassium thiocyanate to give 1-thiocyanato-1,4-diaryl-2,3-diazabutadienes which isomerize thermally to arylideneamino-5-aryl-1,3,4-thiadiazoles. 1-Chloro-1,4-diphenyl-2,3-diazabutadiene reacts with potassium ethylxanthate to give a 1-ethylxanthyl-2,3-diazabutadiene which on pyrolysis yields 2,5-diphenyl-1,3,4-thiadiazole.