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3H-imidazo[4,5-b]pyridine-2-carboxylic acid is a heterocyclic chemical compound with the molecular formula C8H6N2O2. It is a derivative of imidazo[4,5-b]pyridine and features a carboxylic acid group, making it a versatile building block in organic synthesis and medicinal chemistry for the development of pharmaceutical compounds and bioactive molecules.

97640-15-8

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97640-15-8 Usage

Uses

Used in Pharmaceutical Industry:
3H-imidazo[4,5-b]pyridine-2-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds for its ability to form diverse molecular structures that can target specific biological pathways.
Used in Medicinal Chemistry Research:
It serves as a valuable building block for the development of new drugs, contributing to the advancement of medicinal chemistry by enabling the creation of innovative and effective therapeutic agents.
Used in Organic Synthesis:
3H-imidazo[4,5-b]pyridine-2-carboxylic acid is utilized as a reactant in organic synthesis processes, allowing for the formation of complex molecules with potential applications in various fields, including material science and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 97640-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,4 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97640-15:
(7*9)+(6*7)+(5*6)+(4*4)+(3*0)+(2*1)+(1*5)=158
158 % 10 = 8
So 97640-15-8 is a valid CAS Registry Number.

97640-15-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-imidazo[4,5-b]pyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3H-imidazo[4,5-b]pyridine-2-carboxylic acid

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:97640-15-8 SDS

97640-15-8Downstream Products

97640-15-8Relevant academic research and scientific papers

AZAINDOLE CARBOXAMIDES

-

Page/Page column 31, (2010/11/30)

The invention relates to azaindole derivatives of general formula (I), wherein X represents a group of general formula (X1). Said compounds have a therapeutic potential in the treatment of diseases that are accompanied by an impaired dopamine metabolism a

Quinuclidine-substituted hetero-bicyclic aromatic compounds for the treatment of disease

-

, (2008/06/13)

The invention provides compounds of Formula I: wherein W0 is a bicyclic moiety and is These compounds may be in the form of pharmaceutical salts or compositions, may be in pure enantiomeric form or racemic mixtures, and are useful to treat diseases or conditions in which α7 is known to be involved.

Synthesis and some reactions of 2-acetylimidazo[4,5-b]pyridine. Antituberculotic activity of the obtained compounds

Bukowski,Janowiec,Zwolska-Kwiek,Andrzejczyk

, p. 651 - 654 (2007/10/03)

2-Acetylimidazo[4,5-b]pyridine was prepared and its reactions with some aromatic amines and sulfur (Willgerodt-Kindler reaction), some aromatic aldehydes, some carboxylic acid hydrazides as well as thiourea were investigated. New imidazo[4,5-b]pyridine derivatives with different substituents in 2-position (N-arylthioamides, imines, α β-unsaturated ketones, hydrazido-hydrazones and aminothiazole) were obtained. Most of the synthesized compounds were tested in vitro for their antituberculotic activity.

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