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2-(Pyridin-3-yl)oxazolo[4,5-b]pyridine is a heterocyclic chemical compound characterized by the molecular formula C11H6N2O. It features both pyridine and oxazole rings, which contribute to its unique structure and potential reactivity. 2-(Pyridin-3-yl)oxazolo[4,5-b]pyridine has garnered attention in the field of medicinal chemistry due to its potential biological activity and its utility as a building block for the synthesis of pharmaceuticals and bioactive molecules. The distinctive structural attributes and prospective medicinal applications of 2-(Pyridin-3-yl)oxazolo[4,5-b]pyridine render it a compelling subject for ongoing research and development in drug discovery and design.

52333-48-9

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52333-48-9 Usage

Uses

Used in Medicinal Chemistry:
2-(Pyridin-3-yl)oxazolo[4,5-b]pyridine is utilized as a key intermediate in the synthesis of various pharmaceuticals and bioactive molecules. Its unique structure allows for the creation of compounds with specific biological activities, making it a valuable component in the development of new drugs.
Used in Drug Discovery and Design:
In the pharmaceutical industry, 2-(Pyridin-3-yl)oxazolo[4,5-b]pyridine is employed as a scaffold for designing novel drug candidates. Its heterocyclic nature and the presence of both pyridine and oxazole rings provide a versatile platform for chemical modifications, which can enhance the compound's pharmacological properties and target specific biological pathways.
Used in Research and Development:
2-(Pyridin-3-yl)oxazolo[4,5-b]pyridine serves as a subject of interest in academic and industrial research settings. Its exploration is crucial for understanding its potential biological activities and for identifying new therapeutic applications, thereby contributing to the advancement of medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 52333-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,3 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52333-48:
(7*5)+(6*2)+(5*3)+(4*3)+(3*3)+(2*4)+(1*8)=99
99 % 10 = 9
So 52333-48-9 is a valid CAS Registry Number.

52333-48-9SDS

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 2-pyridin-3-yl-[1,3]oxazolo[4,5-b]pyridine

1.2 Other means of identification

Product number -
Other names 2-(Pyridin-3-yl)oxazolo[4,5-b]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:52333-48-9 SDS

52333-48-9Downstream Products

52333-48-9Relevant academic research and scientific papers

New access to oxazolopyridines via hydroxyamidine derivatives; application to quinolines

Garnier, Ethel,Blanchard, Stephanie,Rodriguez, Ivan,Jarry, Christian,Leger, Jean-Michel,Caubere, Paul,Guillaumet, Gerald

, p. 2033 - 2040 (2007/10/03)

Several 2-aryl and 2-heteroaryloxazolo[4,5-b]pyridines were synthesised in high yields from zwitterion or hydroxyamidine derivatives by heating in dimethylacetamide. These intermediates were generated via hetarynic reaction with the complex base NaNH2-t-BuONa (5:2). The same reactions were possible with quinoline derivatives.

Anti-inflammatory oxazole[4,5-b]pyridines

-

, (2008/06/13)

The various isomers of oxazolo- and thiazolopyridines having utility as antiinflammatory, antipyretic and analgesic agents are prepared by condensation of an appropriate amino-hydroxypyridine or amino-mercaptopyridine with a carboxylic acid, halide or anhydride.

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