Cas 1196445-71-2,4-(7-amino-2-hydroxy-5-oxo-6-phenylazo-4,5-dihydropyrazolo[1,5-a]pyrimidin-3-ylazo)-N-[2-(saccharin-2-yl)acetyl]benzenesulfonamide

1196445-71-2

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Basic information

Product Name: 4-(7-amino-2-hydroxy-5-oxo-6-phenylazo-4,5-dihydropyrazolo[1,5-a]pyrimidin-3-ylazo)-N-[2-(saccharin-2-yl)acetyl]benzenesulfonamide
Synonyms:
CAS NO:1196445-71-2
Molecular Formula:
Molecular Weight: 676.65
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: 4-(7-amino-2-hydroxy-5-oxo-6-phenylazo-4,5-dihydropyrazolo[1,5-a]pyrimidin-3-ylazo)-N-[2-(saccharin-2-yl)acetyl]benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-(7-amino-2-hydroxy-5-oxo-6-phenylazo-4,5-dihydropyrazolo[1,5-a]pyrimidin-3-ylazo)-N-[2-(saccharin-2-yl)acetyl]benzenesulfonamide(1196445-71-2)
EPA Substance Registry System: 4-(7-amino-2-hydroxy-5-oxo-6-phenylazo-4,5-dihydropyrazolo[1,5-a]pyrimidin-3-ylazo)-N-[2-(saccharin-2-yl)acetyl]benzenesulfonamide(1196445-71-2)

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: 1196445-71-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1196445-71-2 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, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1196445-71:
(9*1)+(8*1)+(7*9)+(6*6)+(5*4)+(4*4)+(3*5)+(2*7)+(1*1)=182
182 % 10 = 2
So 1196445-71-2 is a valid CAS Registry Number.

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1196445-71-2Relevant 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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