77441-94-2

Upstream product

• 79-19-6 thiosemicarbazide 
• 18692-67-6 2-Phenyl-4-(p-acetylaminobenzyliden)-5-oxazolon 
• 77441-93-1 C₁₀H₁₂N₄O₂S 
• 6296-41-9 p-Aminophenylbrenztraubensaeurehydrochlorid 
• 556-18-3 4-aminobenzaldehyde 
• 16921-36-1 3-(4-aminophenyl)-2-oxopropanoic acid 

Downstream Products

• 77442-00-3 4-(2-Thio-6-azauracil-5-yl-methyl)phenylhydrazonocyanacetylcarbamidsaeureethylester 
• 77441-95-3 2-Thio-5-(4-acetylaminobenzyl)-6-azauracil 
• 112517-76-7 6-(4-Amino-benzyl)-2H-[1,2,4]triazine-3,5-dithione 
• 77441-96-4 3-Methylmercapto-6-(4-aminobenzyl)-2,5-dihydro-1,2,4-triazin-5-on 
• 77441-99-7 4-(6-Azauracil-5-yl-methyl)phenylhydrazonocyanacetylcarbamidsaeureethylester 
• 77442-02-5 2-Thio-5-<4-(5-cyan-6-azauracil-1-yl)benzyl>-6-azauracil 
• 77442-04-7 2-Thio-5-<4-(5-carboxy-6-azauracil-1-yl)benzyl>-6-azauracil 
• 77442-01-4 5-<4-(5-Cyan-6-azauracil-1-yl)benzyl>-6-azauracil 
• 77442-03-6 5-<4-(5-Carboxy-6-azauracil-1-yl)benzyl>-6-azauracil 
• 77441-97-5 3-Methylmercapto-6-(4-acetylaminobenzyl)-2,5-dihydro-1,2,4-triazin-5-on 
• 77441-98-6 5-(4-Aminobenzyl)-6-azauracil 

Relevant academic research and scientific papers

Synthesis and Antimicrobial Activity of 6-Benzyl/p-substituted-benzyl-1,2,4-triazine-3,5-(2H,4H)-dithione

6-Benzyl-1,2,4-triazine-3,5-(2H,4H)-dithione (IIa) and its p-substituted benzyl derivatives (IIb-d) have been prepared from benzaldehyde and substituted benzaldehydes respectively.The compounds have been characterised on the basis of spectral data (UV, IR, PMR and mass) and have also been tested for their antimicrobial activity against a number of bacteria.