85102-27-8

Basic information

• Product Name: IMidazo[1,2-a]pyridine, 7-phenyl-
• Synonyms: IMidazo[1,2-a]pyridine, 7-phenyl-;7-Phenylimidazo[1,2-a]pyridine
• CAS NO: 85102-27-8
• Molecular Formula: C₁₃H₁₀N₂
• Molecular Weight: 194.2319
• Mol File: 85102-27-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: IMidazo[1,2-a]pyridine, 7-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: IMidazo[1,2-a]pyridine, 7-phenyl-(85102-27-8)
• EPA Substance Registry System: IMidazo[1,2-a]pyridine, 7-phenyl-(85102-27-8)

Safety Data

• Hazardous Substances Data: 85102-27-8(Hazardous Substances Data)

Usage

General Description

Imidazo[1,2-a]pyridine, 7-phenyl- is a chemical compound with the molecular formula C13H9N. It is a derivative of imidazopyridine and contains a phenyl group at the seventh position. Imidazo[1,2-a]pyridine, 7-phenyl- is known for its potential pharmaceutical and biological applications, particularly in the field of medicinal chemistry. It has been studied for its potential as a drug candidate for various therapeutic indications, including antiviral, antibacterial, and anticancer activities. Imidazo[1,2-a]pyridine, 7-phenyl- is of interest to researchers and chemists seeking to explore its potential as a novel pharmaceutical agent.

Upstream product

• 85102-40-5 2-Morpholinomethyl-1-(3-phenyl-2-propynyl)-imidazole 
• 107-20-0 2-chloroethanal 
• 60781-83-1 4-phenyl-pyridin-2-ylamine 
• 4532-25-6 7-chloroimidazo-[1,2-a]pyridine 
• 98-80-6 phenylboronic acid 
• 19798-80-2 2-Amino-4-chloropyridine 
• 622402-25-9 tert-butyl (4-phenylpyridin-2-yl)carbamate 
• 405939-28-8 (4-iodopyridin-2-yl)carbamic acid tert-butyl ester 
• 17157-48-1 bromoacetaldehyde 

Downstream Products

• 622402-28-2 7-phenyl-3-pyridin-4-yl-imidazo[1,2-a]pyridine 
• 622402-26-0 3-iodo-7-phenyl-imidazo[1,2-a]pyridine 

Relevant articles and documents

Pd-Catalyzed Tandem Cyclization via C-H Arylation and Acylation for the Construction of Polycyclic Scaffolds

The first Pd-catalyzed tandem cyclization of imidazo[1,2-a]pyridines with 2-chlorobenzaldehydes through C-H arylation and acylation is presented for the efficient synthesis of novel 6H-benzo[b]imidazo[5,1,2-de]quinolizin-6-ones. The direct acylation react

Design and synthesis of 3,7-diarylimidazopyridines as inhibitors of the VEGF-receptor KDR

3,7-Diarylsubstituted imidazopyridines were designed and developed as a new class of KDR kinase inhibitors. A variety of imidazopyridines were synthesized and potent inhibitors of KDR kinase activity were identified with good aqueous solubility.