116221-92-2

Upstream product

• 6292-71-3 4-methoxybenzaldehyde semicarbazone 
• 5711-61-5 2-amino-5-(4-methoxyphenyl)-1,3,4-oxadiazole 
• 75-15-0 carbon disulfide 
• 89335-11-5 N¹-(5-p-methoxyphenyl-1,3,4-oxadiazol-2-yl)thiourea 

Downstream Products

• 521098-73-7 Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[2-(4-methoxy-phenyl)-5,7-dithioxo-7H-[1,3,4]oxadiazolo[3,2-a][1,3,5]triazin-6-yl]-tetrahydro-pyran-3-yl ester 
• 521098-77-1 Acetic acid (2R,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[2-(4-methoxy-phenyl)-5,7-dithioxo-7H-[1,3,4]oxadiazolo[3,2-a][1,3,5]triazin-6-yl]-tetrahydro-pyran-3-yl ester 
• 521098-75-9 acetic acid 4,5-diacetoxy-2-[2-(4-methoxy-phenyl)-5,7-dithioxo-7H-[1,3,4]oxadiazolo[3,2-a][1,3,5]triazin-6-yl]-tetrahydro-pyran-3-yl ester 
• 116221-97-7 2-p-methoxyphenyl-6-(2-methyl-5-fluorophenyl)-1,3,4-oxadiazolo<3,2-a>-s-triazine-5,7-dithione 
• 116236-34-1 2-p-methoxyphenyl-6-p-fluorophenylsulphonyl-1,3,4-oxadiazolo<3,2-a>-s-triazine-5,7-dithione 

Relevant academic research and scientific papers

Synthesis and bioevaluation of some novel nucleosides as antiherptic agents

N1-(5-Aryl-1,3,4-oxadiazolo-2-yl)-ureas on cyclocondensation with CS2/KOH afford 2-aryl-1,3,4-oxadiazole[3,2-a]-s-triazine-5,7-(6H) dithione nucleobase which on glycosylation with different sugars gives nucleoside analogues.

Synthesis and Fungitoxicity of New 1,3,4-Oxadiazolo-s-triazine-5,7-diones and Their Thione Analogues

N1-(5-Aryl-1,3,4-oxadiazol-2-yl)-N3-(4-fluorophenyl)ureas (IIIa-c) on cyclocondensation with ethyl chloroformate and CS2/KOH afford 2-aryl-6-(4-fluorophenyl)-1,3,4-oxadiazolo-s-triazine-5,7-diones (IVa-c) and their 5-thione an