Cas 1196445-56-3,ethyl 6-cyano-5-oxo-3-phenyl-2-{4-[2-(saccharin-2-yl)acetylsulfamoyl]phenyl}-2,5-dihydropyridazine-4-carboxylate

1196445-56-3

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Basic information

Product Name: ethyl 6-cyano-5-oxo-3-phenyl-2-{4-[2-(saccharin-2-yl)acetylsulfamoyl]phenyl}-2,5-dihydropyridazine-4-carboxylate
Synonyms:
CAS NO:1196445-56-3
Molecular Formula:
Molecular Weight: 647.646
EINECS: N/A
Product Categories: N/A

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: ethyl 6-cyano-5-oxo-3-phenyl-2-{4-[2-(saccharin-2-yl)acetylsulfamoyl]phenyl}-2,5-dihydropyridazine-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 6-cyano-5-oxo-3-phenyl-2-{4-[2-(saccharin-2-yl)acetylsulfamoyl]phenyl}-2,5-dihydropyridazine-4-carboxylate(1196445-56-3)
EPA Substance Registry System: ethyl 6-cyano-5-oxo-3-phenyl-2-{4-[2-(saccharin-2-yl)acetylsulfamoyl]phenyl}-2,5-dihydropyridazine-4-carboxylate(1196445-56-3)

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: 1196445-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1196445-56-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,4,4 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1196445-56:
(9*1)+(8*1)+(7*9)+(6*6)+(5*4)+(4*4)+(3*5)+(2*5)+(1*6)=183
183 % 10 = 3
So 1196445-56-3 is a valid CAS Registry Number.

1196445-56-3Upstream product

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1196445-56-3Relevant academic research and scientific papers

Ethyl {4-[2-(saccharin-2-yl)acetylsulfamoyl]phenylazo}cyanoacetate in the synthesis of polyfunctionally heteroaromatic derivatives

Aly

experimental part, p. 895 - 902 (2010/01/11)

(Chemical Equation Presented) An efficient and direct one-pot reaction of ethyl saccharinylcyanoacetate derivative 3 with a variety of active methylene reagents and nitrogen nucleophiles afforded novel series of polyfunctionally substituted heteroaromatic

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