112581-60-9

Basic information

• Product Name: 2,6-DICHLOROIMIDAZO[1,2-A]PYRIDINE
• Synonyms: 2,6-DICHLOROIMIDAZO[1,2-A]PYRIDINE;IMidazo[1,2-a]pyridine, 2,6-dichloro-
• CAS NO: 112581-60-9
• Molecular Formula: C7H4Cl2N2
• Molecular Weight: 187.03
• EINECS: 604-604-1
• Mol File: 112581-60-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,6-DICHLOROIMIDAZO[1,2-A]PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DICHLOROIMIDAZO[1,2-A]PYRIDINE(112581-60-9)
• EPA Substance Registry System: 2,6-DICHLOROIMIDAZO[1,2-A]PYRIDINE(112581-60-9)

Safety Data

• Hazardous Substances Data: 112581-60-9(Hazardous Substances Data)

Usage

General Description

2,6-Dichloroimidazo[1,2-a]pyridine is a chemical compound with the molecular formula C7H3Cl2N3. It is a heterocyclic compound that is used in the synthesis of various pharmaceuticals and agrochemicals. 2,6-DICHLOROIMIDAZO[1,2-A]PYRIDINE is known to have antimicrobial and antiparasitic properties, making it useful in the development of new drugs for the treatment of infectious diseases. It has also been studied for its potential use in the treatment of cancer and other neoplastic diseases. Additionally, it has been investigated for its potential use as a catalyst in organic synthesis reactions. Its unique structure and versatile reactivity make 2,6-dichloroimidazo[1,2-a]pyridine a valuable building block in the development of new chemical compounds with diverse biological and industrial applications.

Upstream product

• 1072-98-6 5-chloro-2-pyridylamine 

Related news

The condensation of 2,6-dichloroimidazo[1,2-a]pyridine with ribonolactone gives a novel imidazo[1,2-a]pyridine C-nucleoside with an unexpected site of ribosylation07/22/2019

A novel ribosylated imidazo[1,2-a]pyridine C-nucleoside was synthesized by condensing a lithiated 2,6-dichloroimidazo[1,2-a]pyridine (1) with a protected ribonolactone (2), followed by acetylation to give the intermediate nucleoside 4. This intermediate was reductively deacetoxylated and deprote...detailed

Relevant articles and documents

An improved synthesis of 2-chlorinated imidazo[1,2-a]pyridines and the application of this procedure for the synthesis of several new polychlorinated imidazo[1,2-a]pyridines

Polychlorinated imidazo[1,2-a]pyridines were synthesized as analogs of certain chlorinated benzimidazoles. The imidazo[1,2-a]pyridines were obtained by a condensation of ethyl bromoacetate and chlorinated 2-aminopyridines. These condensation products were treated with an ion exchange resin to effect an exchange of hydrobromide salts with hydrochloride salts. These compounds were subsequently treated with POCl3 to convert the imidazo[1,2-a]pyridin-2-ones into 2-chloroimidazo[1,2-a]pyridines.

Imidazo[1,2-a]pyridine C-nucleosides as antiviral agents

This invention pertains to nucleoside analogs that have antiviral activity and improved metabolic stability, compositions comprising them, and methods of antiviral treatment employing them. More particularly, this invention pertains to imidazo[1,2-a]pyridine C-nucleosides, as exemplified by compounds such as imidazo[l,2-a]pyridine C5-nucleosides and imidazo[1,2-a]pyridine C3-nucleosides, and may be represented by formula (I), wherein exactly one of Q3and Q5is a sugar-like moiety; exactly one of Q3and Q5is —H; and Q2, Q6, Q7and Q8are independently imidazo[1,2-a]pyridine substituents, such as —H, —F, —Cl, —Br and —I.