Cas 52605-76-2,4-{2-[3-methyl-5-oxo-1H-pyrazol-4(5H)-ylidene]hydrazinyl}-N-(pyrimidin-2-yl)benzenesulfonamide

52605-76-2

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Basic information

Product Name: 4-{2-[3-methyl-5-oxo-1H-pyrazol-4(5H)-ylidene]hydrazinyl}-N-(pyrimidin-2-yl)benzenesulfonamide
Synonyms: 4-{2-[3-methyl-5-oxo-1H-pyrazol-4(5H)-ylidene]hydrazinyl}-N-(pyrimidin-2-yl)benzenesulfonamide
CAS NO:52605-76-2
Molecular Formula:
Molecular Weight: 359.368
EINECS: N/A
Product Categories: N/A
Mol File: 52605-76-2.mol
Article Data: 2

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: 4-{2-[3-methyl-5-oxo-1H-pyrazol-4(5H)-ylidene]hydrazinyl}-N-(pyrimidin-2-yl)benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-{2-[3-methyl-5-oxo-1H-pyrazol-4(5H)-ylidene]hydrazinyl}-N-(pyrimidin-2-yl)benzenesulfonamide(52605-76-2)
EPA Substance Registry System: 4-{2-[3-methyl-5-oxo-1H-pyrazol-4(5H)-ylidene]hydrazinyl}-N-(pyrimidin-2-yl)benzenesulfonamide(52605-76-2)

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: 52605-76-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 52605-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,0 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52605-76:
(7*5)+(6*2)+(5*6)+(4*0)+(3*5)+(2*7)+(1*6)=112
112 % 10 = 2
So 52605-76-2 is a valid CAS Registry Number.

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52605-76-2Relevant articles and documents

Pyrazole and Nicotinonitrile Derivatives Synthesized from Sulfa Drugs, and Their Antibacterial Activity

El-Sayed,Moustafa,Fadda,Abd El-Rahman

, p. 339 - 347 (2019/04/13)

Utility of sulfadiazine and sulfaguanidine in synthesis of new series of pyrazoles and 2-pyridones is described. Diazotization of sulfadiazine that results in formation of diazonium salt 2 followed by coupling of the latter with active methylene compounds

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