5319-75-5

Upstream product

• 5319-77-7 2-amino-5-methylthio-1,3,4-thiadiazole 
• 98-88-4 benzoyl chloride 
• 33949-90-5 4-benzoyl-1-(N'-phenyl-hydrazinothiocarbonyl)-thiosemicarbazide 
• 74-88-4 methyl iodide 
• 33949-82-5 1-hydrazinothiocarbonyl-4-benzoyl-thiosemicarbazide 
• 33949-93-8 1-benzylidenehydrazinothiocarbonyl-4-benzoyl-thiosemicarbazide 
• 33985-59-0 4,4'-dibenzoyl-1,1'-thiocarbonyl-bis-thiosemicarbazide 
• 109853-19-2 C₁₅H₁₄N₄OS₂ 
• 33949-86-9 N-(5-mercapto-1,3,4-thiadiazol-2-yl)benzamide 

Downstream Products

• 1356861-65-8 N-(3-thioxo-2,3-dihydro-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)benzamide 
• 28938-29-6 N-(5-hydrazino-1,3,4-thiadiazol-2-yl)benzamide 
• 34240-11-4 N-(5-methanesulfonyl-[1,3,4]thiadiazol-2-yl)-benzamide 

Relevant academic research and scientific papers

Antimicrobial activity of newly synthesized 2,5-disubstituted 1,3,4-thiadiaozle derivatives

A number of new 2,5-disubstituted 1,3,4-thiadiazole and their S- or N-substituted derivatives as well as the corresponding sugar hydrazone derivatives were synthesized and tested for their antimicrobial activity against Bacillus subtilis (Gram-positive),

A new route to 1,2,4-triazoles and 1,3,4-thiadiazoles from 1-acylbithiourea

The intramolecular cyclization of 1-acylbithiourea 1 gave 1,2,4-triazole 2 and 1,3,4-thiadiazole 3. The reaction of 1 with p-toluenesulfonyl chloride in the presence of triethylamine afforded 3. Treatment of 1 with methyl iodide in the absence of any base yielded 2-methylthio-1,3,4-thiadiazole 10 and 2-imino-1,3,4-thiadiazoline 12.