Cas 556066-76-3,5-methyl-pyridine-2-sulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-(3,4,5-trimethoxy-phenyl)-pyrimidin-4-yl]-amide

556066-76-3

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Basic information

Product Name: 5-methyl-pyridine-2-sulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-(3,4,5-trimethoxy-phenyl)-pyrimidin-4-yl]-amide
Synonyms:
CAS NO:556066-76-3
Molecular Formula:
Molecular Weight: 573.026
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-methyl-pyridine-2-sulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-(3,4,5-trimethoxy-phenyl)-pyrimidin-4-yl]-amide(CAS DataBase Reference)
NIST Chemistry Reference: 5-methyl-pyridine-2-sulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-(3,4,5-trimethoxy-phenyl)-pyrimidin-4-yl]-amide(556066-76-3)
EPA Substance Registry System: 5-methyl-pyridine-2-sulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-(3,4,5-trimethoxy-phenyl)-pyrimidin-4-yl]-amide(556066-76-3)

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: 556066-76-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 556066-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,0,6 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 556066-76:
(8*5)+(7*5)+(6*6)+(5*0)+(4*6)+(3*6)+(2*7)+(1*6)=173
173 % 10 = 3
So 556066-76-3 is a valid CAS Registry Number.

556066-76-3Upstream product

556066-76-3Downstream Products

556066-97-8 5-methyl-pyridine-2-sulfonic acid [6-(2-amino-ethoxy)-5-(2-methoxy-phenoxy)-2-(3,4,5-trimethoxy-phenyl)-pyrimidin-4-yl]-amide

556066-76-3Relevant academic research and scientific papers

Bis-sulfonamides as endothelin receptor antagonists

Boss, Christoph,Bolli, Martin H.,Weller, Thomas,Fischli, Walter,Clozel, Martine

, p. 951 - 954 (2003)

Modification of the structure of bosentan 1, the first marketed endothelin receptor antagonist (Tracleer), by introduction of a second sulfonamide function at the alkoxy side chain, led to bis-sulfonamides 2. This allowed to prepare dual ETA/ETB as well as ETB receptor selective antagonists, which could serve as tools to investigate the pharmacological consequences of selective ETB receptor blockade.

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