Cas 38560-65-5,1,2,4-Triazine-3,5(2H,4H)-dione, 2-[4-[(2-methylphenyl)sulfonyl]phenyl]-

38560-65-5

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Basic information

Product Name: 1,2,4-Triazine-3,5(2H,4H)-dione, 2-[4-[(2-methylphenyl)sulfonyl]phenyl]-
Synonyms:
CAS NO:38560-65-5
Molecular Formula: C16H13N3O4S
Molecular Weight: 343.363
EINECS: N/A
Product Categories: N/A
Mol File: 38560-65-5.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1,2,4-Triazine-3,5(2H,4H)-dione, 2-[4-[(2-methylphenyl)sulfonyl]phenyl]-(CAS DataBase Reference)
NIST Chemistry Reference: 1,2,4-Triazine-3,5(2H,4H)-dione, 2-[4-[(2-methylphenyl)sulfonyl]phenyl]-(38560-65-5)
EPA Substance Registry System: 1,2,4-Triazine-3,5(2H,4H)-dione, 2-[4-[(2-methylphenyl)sulfonyl]phenyl]-(38560-65-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 38560-65-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 38560-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,5,6 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38560-65:
(7*3)+(6*8)+(5*5)+(4*6)+(3*0)+(2*6)+(1*5)=135
135 % 10 = 5
So 38560-65-5 is a valid CAS Registry Number.

38560-65-5Upstream product

76590-35-7 4-((2-methylphenyl)thio)aniline

38560-65-5Downstream Products

38560-65-5Relevant 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

Miller, Max W.,Mylari, Banavara L.,Howes, Harold L.,Figdor, Stanford K.,Lynch, Martin J.,et al.

, p. 1337 - 1342 (2007/10/02)

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

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