53266-59-4

Basic information

• Product Name: {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
• CAS NO: 53266-59-4
• Molecular Weight: 495.343
• Mol File: 53266-59-4.mol

Chemical Properties

• CAS DataBase Reference: {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(CAS DataBase Reference)
• NIST Chemistry Reference: {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(53266-59-4)
• EPA Substance Registry System: {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(53266-59-4)

Safety Data

• Hazardous Substances Data: 53266-59-4(Hazardous Substances Data)

Upstream product

• 99-52-5 2-methyl-4-nitro-benzenamine 
• 78983-80-9 3-chloro-4-<(p-chlorophenyl)thio>-5-methylnitrobenzene 
• 53266-62-9 3-chloro-4-<(p-chlorophenyl)thio>-5-methylaniline 
• 69951-02-6 2-chloro-6-methyl-4-nitro-phenylamine 
• 51719-46-1 1,2-dichloro-3-methyl-5-nitrobenzene 
• 53266-64-1 (2-{[3-Chloro-4-(4-chloro-phenylsulfanyl)-5-methyl-phenyl]-hydrazono}-3-ethoxycarbonylamino-3-oxo-propionyl)-carbamic acid ethyl ester 

Downstream Products

• 38560-81-5 2-<3-chloro-4-<(p-chlorophenyl)thio>-5-methylphenyl>-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 
• 40913-55-1 2-<3-chloro-4-<(p-chlorophenyl)thio>-5-methylphenyl>-6-carboxy-as-triazine-3,5(2H,4H)-dione 

Relevant articles and documents

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