42238-73-3

Upstream product

• 1072-71-5 5-mercapto-1,3,4-thiadiazole-2(3H)-thione 
• 106-47-8 4-chloro-aniline 
• 14731-29-4 5-(4-chloro-anilino)-3H-[1,3,4]thiadiazole-2-thione 
• 2131-55-7 4-Chlorophenyl isothiocyanate 
• 714-22-7 S-allyl-N-(4-chlorophenyl)dithiocarbamate 
• 730-12-1 (4-Chloro-phenyl)-dithiocarbamic acid benzyl ester 
• 709-88-6 Ethyl-p-chlorophenyldithiocarbamat 
• 93535-54-7 N,N'-bis(4-chlorophenyl)hydrazine-1,2-dicarbothioamide 
• 880-29-5 1-(4-ethoxyphenyl)thiourea 
• 22814-92-2 4-(p-chlorophenyl)-3-thiosemicarbazide 
• 134252-08-7 1-(4-Ethoxy-phenyl)-2-ethyl-isothiourea 
• 134252-07-6 1-p-chlorophenyl-2-S-ethylisothiourea 

Relevant academic research and scientific papers

Preparation of 2,5-diamino-1,3,4-thiadiazole derivatives using MgO nanoparticles as heterogeneous basic catalysts

Abstract: The synthesis of 2,5-diamino-1,3,4-thiadiazole derivatives was performed via the reaction of dithiocarbamate derivatives and hydrazine sulfate in presence of MgO nanoparticles as heterogeneous catalysts, which were prepared by the sol–gel method

Dithiocarbamates as an efficient intermediate for the synthesis of symmetrical substituted 2,5-diamino-1,3,4-thiadiazoles in water

Synthesis of symmetrical substituted 2,5-diamino-1,3,4-thiadiazoles is described. Reaction of easily prepared dithiocarbamates with hydrazine gives the corresponding thiadiazoles in moderate to good yields. This method is new, efficient, and simple especi

A novel strategy for the construction of azole heterocycles via an oxidative desulfurization approach using iodobenzene and oxone

The oxidative desulfurization approach has been utilized for the construction of oxadiazole and thiadiazole heterocycles using iodobenzene and Oxone. The use of iodobenzene and the inexpensive readily available oxidant Oxone makes the reaction system simp