97640-15-8

Basic information

• Product Name: 3H-imidazo[4,5-b]pyridine-2-carboxylic acid
• Synonyms: 3H-imidazo[4,5-b]pyridine-2-carboxylic acid;1H-Imidazo[4,5-b]pyridine-2-carboxylic acid
• CAS NO: 97640-15-8
• Molecular Formula: C7H5N3O2
• Molecular Weight: 163.1335
• Mol File: 97640-15-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3H-imidazo[4,5-b]pyridine-2-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-imidazo[4,5-b]pyridine-2-carboxylic acid(97640-15-8)
• EPA Substance Registry System: 3H-imidazo[4,5-b]pyridine-2-carboxylic acid(97640-15-8)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 97640-15-8(Hazardous Substances Data)

Usage

General Description

3H-imidazo[4,5-b]pyridine-2-carboxylic acid is a chemical compound with the molecular formula C8H6N2O2. It is a heterocyclic compound that contains both nitrogen and oxygen atoms. 3H-imidazo[4,5-b]pyridine-2-carboxylic acid is a derivative of imidazo[4,5-b]pyridine and contains a carboxylic acid group. It is used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceutical compounds. The structure of 3H-imidazo[4,5-b]pyridine-2-carboxylic acid makes it a versatile compound for the development of new drugs and other bioactive molecules.

Upstream product

• 250651-52-6 2-(1-hydroxyethyl)-1H-imidazo[4,5-b]pyridine 
• 452-58-4 2,3-Diaminopyridine 
• 79-14-1 glycolic Acid 
• 24638-20-8 (3H-imidazo[4,5-b]pyridin-2-yl)methanol 

Relevant articles and documents

AZAINDOLE CARBOXAMIDES

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

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

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.