100592-11-8

Basic information

• Product Name: 8-Hydroxyimidazo[1,2-a]pyridine, HCl
• Synonyms: 8-Hydroxyimidazo[1,2-a]pyridine, HCl;Imidazo[1,2-a]pyridin-8-ol, HCl;8-Hydroxyimidazo[1,2-a]pyridinehydrochloride97%
• CAS NO: 100592-11-8
• Molecular Formula: C7H7ClN2O
• Molecular Weight: 170.6
• Product Categories: blocks;Imidazoles;Pyridines
• Mol File: 100592-11-8.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 8-Hydroxyimidazo[1,2-a]pyridine, HCl(CAS DataBase Reference)
• NIST Chemistry Reference: 8-Hydroxyimidazo[1,2-a]pyridine, HCl(100592-11-8)
• EPA Substance Registry System: 8-Hydroxyimidazo[1,2-a]pyridine, HCl(100592-11-8)

Safety Data

• Hazardous Substances Data: 100592-11-8(Hazardous Substances Data)

Usage

Uses

Used in Chelating Applications:
8-Hydroxyimidazo[1,2-a]pyridine, HCl is utilized as a chelating agent in various industrial and laboratory applications. Its ability to form stable complexes with metal ions makes it suitable for metal extraction and purification processes, enhancing the efficiency and selectivity of these operations.
Used in Pharmaceutical Production:
8-Hydroxyimidazo[1,2-a]pyridine, HCl is employed in the production of pharmaceuticals due to its potential therapeutic properties. Its antimicrobial and anti-inflammatory characteristics make it a valuable component in the development of new drugs targeting a range of health conditions.
Used as a Catalyst in Organic Synthesis:
8-Hydroxyimidazo[1,2-a]pyridine, HCl also serves as a catalyst in organic synthesis reactions. Its unique structure allows it to facilitate and accelerate chemical reactions, improving the yield and efficiency of synthetic processes in the chemical and pharmaceutical industries.

Upstream product

• 107-20-0 2-chloroethanal 
• 16867-03-1 2-amino-3-hydroxypyridine 
• 96428-16-9 8-(phenylmethoxy)imidazo[1,2-a]pyridine 
• 71-36-3 butan-1-ol 

Downstream Products

• 69214-22-8 8-hydroxy-imidazo<1,2-a>pyridine 

Relevant articles and documents

3-Condensed imidazolium-cephem compounds

A compound of the formula; STR1 wherein R1 is an amino group which may be protected, R3 is a hydrogen atom or an optionally substituted hydrocarbon residue; Z is S, S→O, O or CH2, R4 is a hydrogen atom, methoxy

Cephalosporin compounds

A compound of the formula; STR1 wherein R0 stands for hydrogen atom, nitrogen-containing heterocyclic group, acyl group or esterified carboxyl group, Z stands for S, S→O, O or CH2, R4 stands for hydrogen atom, methoxy grou

SYNTHESIS OF NEW HETEROCYCLIC PHENOLS: 8-HYDROXY-IMIDAZOPYRIDINE

Preparation of the unknown title compound has been achieved by condensation of 2-amino-3-hydroxy-pyridine with chloroacetaldehyde.Activation by the free phenolic hydroxyl allows preferential nitration of the pyridine ring, in marked contrast to the behavior of the related ethers which suffer electrophilic substitution on the imidazole moiety, as usual in the series.