Cas 181272-13-9,5-chloro-2-methoxy-<i>N</i>-(2-{4-[2-(2-methoxy-ethoxy)-ethoxy]-3-sulfamoyl-phenyl}-ethyl)-benzamide

181272-13-9

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Basic information

Product Name: 5-chloro-2-methoxy-N-(2-{4-[2-(2-methoxy-ethoxy)-ethoxy]-3-sulfamoyl-phenyl}-ethyl)-benzamide
Synonyms: 5-chloro-2-methoxy-N-(2-{4-[2-(2-methoxy-ethoxy)-ethoxy]-3-sulfamoyl-phenyl}-ethyl)-benzamide
CAS NO:181272-13-9
Molecular Formula:
Molecular Weight: 486.974
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: 5-chloro-2-methoxy-N-(2-{4-[2-(2-methoxy-ethoxy)-ethoxy]-3-sulfamoyl-phenyl}-ethyl)-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: 5-chloro-2-methoxy-N-(2-{4-[2-(2-methoxy-ethoxy)-ethoxy]-3-sulfamoyl-phenyl}-ethyl)-benzamide(181272-13-9)
EPA Substance Registry System: 5-chloro-2-methoxy-N-(2-{4-[2-(2-methoxy-ethoxy)-ethoxy]-3-sulfamoyl-phenyl}-ethyl)-benzamide(181272-13-9)

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: 181272-13-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 181272-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,2,7 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 181272-13:
(8*1)+(7*8)+(6*1)+(5*2)+(4*7)+(3*2)+(2*1)+(1*3)=119
119 % 10 = 9
So 181272-13-9 is a valid CAS Registry Number.

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181272-13-9Relevant academic research and scientific papers

Cardioselective KATP channel blockers derived from a new series of m-anisamidoethylbenzenesulfonylthioureas

Englert,Gerlach,Goegelein,Hartung,Heitsch,Mania,Scheidler

, p. 1085 - 1098 (2007/10/03)

Sulfonylthioureas exhibiting cardioselective blockade of ATP-sensitive potassium channels (KATP channels) were discovered by stepwise structural variations of the antidiabetic sulfonylurea glibenclamide. As screening assays, reversal of rilmaka

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