53266-64-1

Upstream product

• 49754-15-6 malonyldiurethane 
• 53266-62-9 3-chloro-4-<(p-chlorophenyl)thio>-5-methylaniline 
• 99-52-5 2-methyl-4-nitro-benzenamine 
• 78983-80-9 3-chloro-4-<(p-chlorophenyl)thio>-5-methylnitrobenzene 
• 69951-02-6 2-chloro-6-methyl-4-nitro-phenylamine 

Downstream Products

• 53266-59-4 {2-[3-chloro-4-(4-chloro-phenylsulfanyl)-5-methyl-phenyl]-3,5-dioxo-2,3,4,5-tetrahydro-[1,2,4]triazine-6-carbonyl}-carbamic acid ethyl ester 
• 38560-81-5 2-<3-chloro-4-<(p-chlorophenyl)thio>-5-methylphenyl>-as-triazine-3,5(2H,4H)-dione 
• 40913-55-1 2-<3-chloro-4-<(p-chlorophenyl)thio>-5-methylphenyl>-6-carboxy-as-triazine-3,5(2H,4H)-dione 
• 78983-78-5 2-[3-Chloro-4-(4-chloro-benzenesulfonyl)-5-methyl-phenyl]-2H-[1,2,4]triazine-3,5-dione 

Relevant academic research and scientific papers

Anticoccidial Derivatives of 6-Azauracil. 4. A 1000-fold Enhancement of Potency by Phenyl Sulfide and Phenyl Sulfone Side Chains

We report further progress in exploiting our earlier discovery that the anticoccidial activity of 6-azauracil increases markedly when appropriately substituted benzyl or phenyl groups are attached at N-1.With guidance from previous structure-activity rela