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290815-30-4

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290815-30-4 Usage

Description

N-(6-chloro-5-(2-methoxyphenoxy)-2-(pyridin-4-yl)pyrimidin-4-yl)-5-methylpyridine-2-sulfonamide is a complex organic chemical compound with a unique structure that features a sulfonamide group attached to a pyrimidine and pyridine core. N-(6-chloro-5-(2-Methoxyphenoxy)-2-(pyridin-4-yl)pyriMidin-4-yl)-5-Methylpyridine-2-sulfonaMide has been investigated for its potential pharmacological properties, particularly as a kinase inhibitor, which could make it a candidate for targeted therapy in the treatment of various diseases.

Uses

Used in Pharmaceutical Industry:
N-(6-chloro-5-(2-methoxyphenoxy)-2-(pyridin-4-yl)pyrimidin-4-yl)-5-methylpyridine-2-sulfonamide is used as a potential therapeutic agent for the treatment of various diseases, including cancer and inflammatory conditions. Its structure suggests that it may act as a kinase inhibitor, which could make it a valuable component in targeted therapies for these conditions.
Used in Cancer Treatment:
In the field of oncology, N-(6-chloro-5-(2-methoxyphenoxy)-2-(pyridin-4-yl)pyrimidin-4-yl)-5-methylpyridine-2-sulfonamide is being studied for its potential as a targeted therapy agent. Its kinase inhibitory properties could make it useful in treating various types of cancer by specifically targeting and inhibiting the activity of enzymes involved in cancer cell growth and proliferation.
Used in Inflammatory Condition Treatment:
N-(6-chloro-5-(2-methoxyphenoxy)-2-(pyridin-4-yl)pyrimidin-4-yl)-5-methylpyridine-2-sulfonamide is also being explored for its potential use in treating inflammatory conditions. Its ability to act as a kinase inhibitor may help in managing inflammation by targeting specific enzymes that contribute to the inflammatory response.
Further research is needed to fully understand the potential therapeutic applications of this compound and to determine its safety and efficacy in clinical settings.

Check Digit Verification of cas no

The CAS Registry Mumber 290815-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,8,1 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 290815-30:
(8*2)+(7*9)+(6*0)+(5*8)+(4*1)+(3*5)+(2*3)+(1*0)=144
144 % 10 = 4
So 290815-30-4 is a valid CAS Registry Number.

290815-30-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-pyridine-2-sulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide

1.2 Other means of identification

Product number -
Other names N-(6-chloro-5-(2-methoxyphenoxy)-2-(pyridin-4-yl)pyrimidin-4-yl)-5-methylpyridine-2-sulfonamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:290815-30-4 SDS

290815-30-4Relevant articles and documents

Bis-sulfonamides as endothelin receptor antagonists

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

, p. 951 - 954 (2007/10/03)

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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