754207-98-2

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 13036-92-5 ammonium N-(4-ethoxyphenyl)dithiocarbamate 

Downstream Products

• 30369-87-0 (4,6-dichloro-[1,3,5]triazin-2-yl)-(2-methoxy-phenyl)-amine 
• 62752-06-1 6-Chloro-N,N'-bis-(2-methoxy-phenyl)-[1,3,5]triazine-2,4-diamine 
• 30377-27-6 4,6-dichloro-N-(4-methoxyphenyl)-1,3,5-triazin-2-amine 
• 6737-62-8 6-chloro-N,N'-bis(4-methoxyphenyl)-1,3,5-triazine-2,4-diamine 
• 78912-07-9 6-Chloro-N,N'-bis-(4-ethoxy-phenyl)-[1,3,5]triazine-2,4-diamine 
• 68301-05-3 2,4-dichloro-6-(4-ethoxyanilino)-s-triazine 
• 27327-56-6 2-(3-methylanilino)-4,6-dichloro-1,3,5-triazine 
• 62752-05-0 6-chloro-N,N'-di-m-tolyl-[1,3,5]triazine-2,4-diamine 
• 2272-23-3 (4,6-dichloro-[1,3,5]triazin-2-yl)-o-tolyl-amine 
• 2272-24-4 (4,6-dichloro-[1,3,5]triazin-2-yl)-p-tolyl-amine 

Relevant academic research and scientific papers

Simple and efficient synthetic routes to s-triazinyl dithiocarbamate derivatives: 2,4-Diarylamino-6-[N-(4′ -ethoxyphenyl)dithiocarbamoyl]-s-triazines and 2,4-bis-[N-(4′ -ethoxyphenyl)dithiocarbamoyl]-6-arylamino-s-triazines

Compounds 2,4-diarylamino-6-[N-(4′ -ethoxyphenyl)dithiocarbamoyl]-s-triazines 4a-f and 2,4-bis-[N-(4′ -ethoxyphenyl)dithiocarbamoyl]-6-arylamino-s-triazines 7a-f have been synthesized by two different methods. In the first method (A) of preparation, 2,4,6-trichloro-s-triazine 1 is condensed with N-(4-ethoxyphenyl)ammoniumdithiocarbamate to afford 3 or 6 followed by the reaction with arylamines to afford 4a-f or 7a-f. In the second method (B) of preparation, 1 is condensed with arylamines to yield 2a-f or 5a-f followed by the action of N-(4-ethoxyphenyl)ammoniumdithiocarbamates to yield 4a-f or 7a-f. The constitutions of newly synthesised compounds 4a-f and 7a-f have been established on the basis of elemental analyses, IR and PMR spectral data. Antimicrobial activity of compounds 4a-f and 7a-f are performed by using cup-plate method against gram-positive bacteria, gram-negative bacteria and antifungal fungi. All the synthesised compounds have shown significant antimicrobial activity.