131773-23-4

Basic information

• Product Name: 2-CHLORO-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE
• Synonyms: IFLAB-BB F2124-0672;AURORA KA-4215;2-CHLORO-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE;IMidazo[1,2-a]pyridine-3-carboxaldehyde, 2-chloro-
• CAS NO: 131773-23-4
• Molecular Formula: C8H5ClN2O
• Molecular Weight: 180.59
• Mol File: 131773-23-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Density: 1.42g/cm³
• Refractive Index: 1.662
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-CHLORO-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE(131773-23-4)
• EPA Substance Registry System: 2-CHLORO-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE(131773-23-4)

Safety Data

• Hazardous Substances Data: 131773-23-4(Hazardous Substances Data)

Usage

General Description

2-CHLORO-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE is a chemical compound with a molecular formula C8H5ClN2O. It is an aldehyde derivative with a chloro-substituted imidazo[1,2-a]pyridine ring structure. 2-CHLORO-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE has potential applications in pharmaceutical research and drug development due to its unique chemical properties and structure. It may be used as a building block in the synthesis of various organic compounds, including pharmaceutical intermediates and agrochemicals. Its specific chemical and biological properties make it a valuable target for further exploration in the field of medicinal chemistry and drug design. However, it is important to handle and use this compound with care, as it may have potential health and safety hazards.

InChI:InChI=1/C8H5ClN2O/c9-8-6(5-12)11-4-2-1-3-7(11)10-8/h1-5H

Upstream product

• 68-12-2 N,N-dimethyl-formamide 
• 3999-05-1 2-chloroimidazo[1,2-a]pyridine 
• 126202-06-0 2-(2-imino-1,2-dihydropyridin-1-yl)acetic acid 
• 504-29-0 2-aminopyridine 

Relevant articles and documents

Synthesis and Physicochemical Properties of New Chalcones Containing a 2-Chloroimidazo[1,2-a]pyridine Fragment

Abstract: New chalcones containing a 2-chloroimidazo[1,2-a]pyridine fragment have been synthesized, and their optical properties have been studied. The Stokes shifts, forbidden band gap widths, molar absorption coefficients, and fluorescence quantum yields have been determined on the basis of their absorption and emission spectra. Introduction of an additional thiophene fragment into the chalcone molecules produced an increase of the Stokes shift, red shift of the emission maximum, and sharp increase of the quantum yield (up to 22%). The synthesized chalcones showed high thermal stability and good film-forming properties, and films obtained therefrom exhibited an ordered structure.

Insights into selenylation of imidazo[1,2-a]pyridine: synthesis, structural and antimicrobial evaluation

An efficient methodology was developed to synthesize novel organoselenium derivatives of formyl-substituted imidazo[1,2-a]pyridine by nucleophilic aromatic substitution with aryl selenolate anions generated in situ through the reduction of different disel