950256-52-7

Upstream product

• 619-42-1 4-methoxycarbonylphenyl bromide 
• 5933-32-4 4-bromobenzoic acid hydrazide 
• 85106-56-5 p-bromobenzoylhydrazinyl dithiocarbamate potassium salt 
• 586-76-5 4-Bromobenzoic acid 
• 55-22-1 pyridine-4-carboxylic acid 
• 85106-58-7 4-amino-5-(4-bromophenyl)-2,4-dihydro-3H[1,2,4]triazole-3-thione 

Relevant academic research and scientific papers

Some pyridyl- and thiophenyl- Substituted 1,2,4-triazolo[3,4-b]1,3,4- thiadiazole derivatives as potent antibacterial

The target compounds 6-11a-e were synthesized by condensing 4-amino-5-aryl-3H-1,2,4-triazole-3-thiones 5a-f with various aromatic carboxylic acids in the presence of phosphorous oxychloride. The structures of newly synthesized compounds were characterized by IR, 1H NMR, 13C NMR, elemental analysis and mass spectrometric studies. All the synthesized compounds were screened for their antibacterial activity. Almost all the tested compounds were potent against four different strains of bacteria when compared with that of reference drug ciprofloxacin. Compounds 6c, 6e, 8d, 9b, 9e, 11a and 11b showed nearly equal or lower MIC values than standard drug, against all four tested bacterial strains but rest of the compounds showed excellent antibacterial activities.