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4-Chlorothiazolo[4,5-c]pyridine is a heterocyclic organic compound characterized by the molecular formula C7H4ClN3S. It features a unique structure with a thiazole ring fused to a pyridine ring, which endows it with potential biological and pharmacological activities. 4-Chlorothiazolo[4,5-c]pyridine is of significant interest in the field of organic chemistry, particularly for its role as a kinase inhibitor in various cellular signaling pathways and its potential as a building block in the synthesis of new pharmaceuticals and agrochemicals.

214045-74-6

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214045-74-6 Usage

Uses

Used in Drug Discovery and Development:
4-Chlorothiazolo[4,5-c]pyridine is utilized as a kinase inhibitor in drug discovery and development. Its ability to modulate cellular signaling pathways makes it a promising candidate for the treatment of various diseases, including cancer and inflammatory conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 4-Chlorothiazolo[4,5-c]pyridine serves as an important building block for the production of new pharmaceuticals and agrochemicals. Its unique structure allows for the creation of novel compounds with potential therapeutic applications.
Used in Pharmaceutical Industry:
4-Chlorothiazolo[4,5-c]pyridine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its presence in these molecules can contribute to their biological activity and therapeutic efficacy.
Used in Agrochemical Industry:
4-Chlorothiazolo[4,5-c]pyridine also finds application in the agrochemical industry, where it is used as a precursor for the development of new pesticides and other agrochemical products. Its potential to act as a building block in the synthesis of these compounds can lead to the discovery of more effective and environmentally friendly solutions for agricultural challenges.

Check Digit Verification of cas no

The CAS Registry Mumber 214045-74-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,0,4 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 214045-74:
(8*2)+(7*1)+(6*4)+(5*0)+(4*4)+(3*5)+(2*7)+(1*4)=96
96 % 10 = 6
So 214045-74-6 is a valid CAS Registry Number.

214045-74-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-[1,3]thiazolo[4,5-c]pyridine

1.2 Other means of identification

Product number -
Other names 4-CHLOROTHIAZOLO[4,5-C]PYRIDINE

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:214045-74-6 SDS

214045-74-6Downstream Products

214045-74-6Relevant academic research and scientific papers

Substituted pyridine and pyrimidine derivatives and their use in treating viral infections

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Page/Page column 139; 140, (2016/09/26)

The present invention provides compounds of Formula (I): and tautomers, isomers, and esters of said compounds, and pharmaceutically acceptable salts, solvates, and prodrugs of said compounds, wherein each of R, R1, X, Y, Z, R2, R3, R4, R5, R6, R7, R8, R9, R18, R19 and n is selected independently and as defined herein. Compositions comprising such compounds are also provided. The compounds of the invention are effective as inhibitors of HCV, and are useful, alone and together with other therapeutic agents, in treating or preventing diseases or disorders such as viral infections and virus-related disorders.

Syntheses of 4- and 6-substituted thiazolo[4,5-c]pyridines

Huang, Yuhua,Bennett, Frank,Girijavallabhan, Vinay,Alvarez, Carmen,Chan, Tze-Ming,Osterman, Rebecca,Senior, Mary,Kwong, Cecil,Bansal, Namita,George Njoroge,MacCoss, Malcolm

scheme or table, p. 2800 - 2802 (2010/07/04)

A general synthetic approach to 4,6-substituted thiazole[4,5-c]pyridines, involving a novel one-pot thiol deprotection-cyclization key step, is described.

Novel methods to functionalize thiazolo[4,5-c]pyridines

Girijavallabhan, Vinay,Arasappan, Ashok,Bennett, Frank,Huang, Yuhua,George Njoroge,MacCoss, Malcolm

experimental part, p. 2797 - 2799 (2010/07/04)

Novel substituted thiazole[4,5-c]pyridines have been synthesized in good yields from unsubstituted thiazole[4,5-c]pyridine using direct C-H coupling reactions and N-oxide rearrangement chemistry.

SUBSTITUTED PYRIDINE AND PYRIMIDINE DERIVATIVES AND THEIR USE IN TREATING VIRAL INFECTIONS

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Page/Page column 167-168, (2010/04/03)

The present invention provides compounds of Formula (I): and tautomers, isomers, and esters of said compounds, and pharmaceutically acceptable salts, solvates, and prodrugs of said compounds, wherein wherein each of R, R1, X, Y, Z, R2, R3, R4, R5, R6, R7, R8, R9, R18, R19 and n is selected independently and as defined herein. Compositions comprising such compounds are also provided. The compounds of the invention are effective as inhibitors of HCV, and are useful, alone and together with other therapeutic agents, in treating or preventing diseases or disorders such as viral infections and virus-related disorders.

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