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2-(3-pyridinyl)-3H-imidazo[4,5-b]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71766-33-1

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71766-33-1 Usage

Type of compound

Heterocyclic compound

Structure

Two fused rings and a pyridine group

Biological and pharmacological activities

Potential anti-cancer, anti-inflammatory, and immune-modulating properties

Potential use

Building block in the development of various pharmaceutical drugs

Agonist

Adrenaline receptor

Research interest

Unique structure and potential biological activities make it a compound of interest for further research and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 71766-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,7,6 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71766-33:
(7*7)+(6*1)+(5*7)+(4*6)+(3*6)+(2*3)+(1*3)=141
141 % 10 = 1
So 71766-33-1 is a valid CAS Registry Number.

71766-33-1SDS

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)-3H-imidazo[4,5-b]pyridine

1.2 Other means of identification

Product number -
Other names 2-pyridin-3-yl-1(3)H-imidazo[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:71766-33-1 SDS

71766-33-1Downstream Products

71766-33-1Relevant academic research and scientific papers

Regioselective C2-arylation of imidazo[4,5-b]pyridines

Macdonald, Jonathan,Oldfield, Victoria,Bavetsias, Vassilios,Blagg, Julian

, p. 2335 - 2347 (2013/04/23)

We show that N3-MEM-protected imidazo[4,5-b]pyridines undergo efficient C2-functionalisation via direct C-H arylation. Twenty-two substituted imidazo[4,5-b]pyridines are prepared and iterative, selective elaboration of functionalised imidazo[4,5-b]pyridin

PREPARATION OF 2-ARYL-SUBSTITUTED IMIDAZOPYRIDINES AND IMIDAZOPYRIDINES

Yutilov, Yu. M.,Shcherbina, L. I.

, p. 529 - 535 (2007/10/02)

It is proposed that sulfur be used as the oxidizing agent in the synthesis of 2-arylimidazopyridines from o-diaminopyridines and aromatic (heteroaromatic) aldehydes.Benzyl alcohols and benzylpyridinium salts can be used in place of aldehydes. 2-Phenylimid

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