139022-27-8

Basic information

• Product Name: Imidazo[1,2-a]pyridine, 6-fluoro- (9CI)
• Synonyms: Imidazo[1,2-a]pyridine, 6-fluoro- (9CI);6-fluoroimidazo[1,2-a]pyridine;6-FluoroiMidazole[1,2-a]pyridine;Imidazo[1,2-a]pyridine, 6-fluoro-
• CAS NO: 139022-27-8
• Molecular Formula: C₇H₅FN₂
• Molecular Weight: 136.1264032
• Product Categories: AMINETERTIARY
• Mol File: 139022-27-8.mol
• Article Data: 8

Chemical Properties

• Melting Point: 70-71°
• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: Imidazo[1,2-a]pyridine, 6-fluoro- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Imidazo[1,2-a]pyridine, 6-fluoro- (9CI)(139022-27-8)
• EPA Substance Registry System: Imidazo[1,2-a]pyridine, 6-fluoro- (9CI)(139022-27-8)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 139022-27-8(Hazardous Substances Data)

Usage

General Description

Imidazo[1,2-a]pyridine, 6-fluoro- (9CI) is a chemical compound with the molecular formula C8H6FN. It is a heterocyclic aromatic compound that contains both nitrogen and fluorine atoms. This chemical has potential applications in the field of medicinal chemistry, particularly in the development of pharmaceutical drugs. It may also have uses in the fields of agriculture, materials science, and as a research tool in chemical biology. Its specific properties and potential uses would need to be further investigated through research and testing.

Upstream product

• 21717-96-4 2-amino-5-fluoropyridine 
• 17157-48-1 bromoacetaldehyde 
• 107-20-0 2-chloroethanal 

Downstream Products

• 1219127-01-1 6-fluoro-3-iodoimidazo[1,2-a]pyridine 
• 1235993-30-2 6-fluoro-3-nitro-imidazo[1,2-a]pyridine 
• 1338248-71-7 6-fluoro-3-phenylimidazo[1,2-a]pyridine 

Relevant articles and documents

From Synthetic Simplified Marine Metabolite Analogues to New Selective Allosteric Inhibitor of Aurora B Kinase

Significant inhibition of Aurora B was achieved by the synthesis of simplified fragments of benzosceptrins and oroidin belonging to the marine pyrrole-2-aminoimidazoles metabolites isolated from sponges. Evaluation of kinase inhibition enabled the discovery of a synthetically accessible rigid acetylenic structural analogue EL-228 (1), whose structure could be optimized into the potent CJ2-150 (37). Here we present the synthesis of new inhibitors of Aurora B kinase, which is an important target for cancer therapy through mitosis regulation. The biologically oriented synthesis yielded several nanomolar inhibitors. The optimized compound CJ2-150 (37) showed a non-ATP competitive allosteric mode of action in a mixed-type inhibition for Aurora B kinase. Molecular docking identified a probable binding mode in the allosteric site "F"and highlighted the key interactions with the protein. We describe the improvement of the inhibitory potency and specificity of the novel scaffold as well as the characterization of the mechanism of action.

Heteroaryl imidazolone derivatives as jak inhibitors

New heteroaryl imidazolone derivatives having the chemical structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Janus Kinases (JAK).

IMIDAZOPYRIDINE DERIVATIVES AS JAK INHIBITORS

New imidazopyridine derivatives having the chemical structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Janus Kinases (JAK).