Cas 1217859-27-2,4-(4-amino-2-(dicyanomethylene)thiazol-3-(2H)-yl)-N-(4-methoxy-1,2,5-thiadiazol-3-yl)benzenesulfonamide

1217859-27-2

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Basic information

Product Name: 4-(4-amino-2-(dicyanomethylene)thiazol-3-(2H)-yl)-N-(4-methoxy-1,2,5-thiadiazol-3-yl)benzenesulfonamide
Synonyms: 4-(4-amino-2-(dicyanomethylene)thiazol-3-(2H)-yl)-N-(4-methoxy-1,2,5-thiadiazol-3-yl)benzenesulfonamide
CAS NO:1217859-27-2
Molecular Formula:
Molecular Weight: 433.495
EINECS: N/A
Product Categories: N/A
Mol File: 1217859-27-2.mol
Article Data: 1

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-(4-amino-2-(dicyanomethylene)thiazol-3-(2H)-yl)-N-(4-methoxy-1,2,5-thiadiazol-3-yl)benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-(4-amino-2-(dicyanomethylene)thiazol-3-(2H)-yl)-N-(4-methoxy-1,2,5-thiadiazol-3-yl)benzenesulfonamide(1217859-27-2)
EPA Substance Registry System: 4-(4-amino-2-(dicyanomethylene)thiazol-3-(2H)-yl)-N-(4-methoxy-1,2,5-thiadiazol-3-yl)benzenesulfonamide(1217859-27-2)

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: 1217859-27-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1217859-27-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,8,5 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1217859-27:
(9*1)+(8*2)+(7*1)+(6*7)+(5*8)+(4*5)+(3*9)+(2*2)+(1*7)=172
172 % 10 = 2
So 1217859-27-2 is a valid CAS Registry Number.

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1217859-27-2Relevant articles and documents

Synthesis of thiazolidine and thiophene derivatives for evaluation as anticancer agents

El-Gaby,Ismail,Abdel-Gawad,Aly,Ghorab

experimental part, p. 2645 - 2654 (2010/04/05)

The non-isolated adducts (3a,b) were used as key intermediates to synthesize some novel thiazolidine and thiophene derivatives. Compound (4) exhibited a remarkable antitumor activity against EAC cells compared with the Doxorubicin as a positive control. T

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