214958-27-7

Basic information

• Product Name: 2-(4-IODOPHENYL)IMIDAZO[1,2-A]PYRIDINE
• Synonyms: 2-(4-IODOPHENYL)IMIDAZO[1,2-A]PYRIDINE
• CAS NO: 214958-27-7
• Molecular Formula: C₁₃H₉IN₂
• Molecular Weight: 320.13
• Mol File: 214958-27-7.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-IODOPHENYL)IMIDAZO[1,2-A]PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-IODOPHENYL)IMIDAZO[1,2-A]PYRIDINE(214958-27-7)
• EPA Substance Registry System: 2-(4-IODOPHENYL)IMIDAZO[1,2-A]PYRIDINE(214958-27-7)

Safety Data

• Hazardous Substances Data: 214958-27-7(Hazardous Substances Data)

Usage

General Description

2-(4-Iodophenyl)imidazo[1,2-a]pyridine is a chemical compound with the molecular formula C13H8IN3. It belongs to the class of imidazo[1,2-a]pyridines, which are heterocyclic compounds with a fused imidazole and pyridine ring system. This particular compound contains a phenyl group with an iodine atom attached to the 4-position of the ring. It has potential pharmaceutical applications due to its ability to modulate certain biological pathways, and it is being studied for its potential use in the treatment of various medical conditions. Its specific properties and potential uses are a subject of ongoing research and development.

Upstream product

• 504-29-0 2-aminopyridine 
• 31827-94-8 2-bromo-1-(4-iodophenyl)ethanone 
• 13329-40-3 4-Iodoacetophenone 
• 110-86-1 pyridine 
• 1612760-02-7 1-(4-iodophenyl)ethanone O-acetyl oxime 
• 25309-64-2 4-ethyl-1-iodobenzene 

Downstream Products

• 55843-91-9 4-(H-imidazo[1,2-a]pyridin-2-yl)benzonitrile 
• 118000-48-9 4-imidazo[1,2-a]pyridin-2-ylbenzaldehyde 
• 214958-28-8 (E)-3-(4-Imidazo[1,2-a]pyridin-2-yl-phenyl)-acrylonitrile 
• 214958-51-7 2-{4-[(E)-2-(4,5-Dihydro-thiazol-2-yl)-vinyl]-phenyl}-imidazo[1,2-a]pyridine 
• 1222-57-7 zolimidine 
• 300401-95-0 4-iodo-N-(pyridin-2-yl)benzamide 

Relevant articles and documents

Synthetic method of imidazopyridine compounds

The invention provides a novel method for synthesizing imidazopyridine compounds. According to the invention, aminopyridine compounds and sulfur ylide are used as original reaction substrates, iron phthalocyanine (FeIIPc) is used as a catalyst, and a series of the imidazopyridine compounds are obtained under the condition that the advantages of mildness, greenness, high efficiency, wide substrateuniversality and the like are achieved.

Method for synthesizing 2-arylimidazo[1, 2-a]pyridine compound

The invention discloses a method for synthesizing a 2-arylimidazo[1, 2-a]pyridine compound and belongs to the technical field of organic synthesis. The method comprises that an ethylbenzene compound,dibromohydantoin DBH and t-butyl hydroperoxide TBHP are added into water and undergo a reaction at 60 DEG C, an inorganic base and an alpha-aminopyridine compound are added into the reaction product and the mixture undergoes a reaction at 80 DEG C to produce a desired product 2-arylimidazo[1, 2-a]pyridine compound. The 2-arylimidazo[1, 2-a]pyridine compound is synthesized from the ethylbenzene compound which is cheaper and more readily available than the 2-arylimidazo[1, 2-a]pyridine compounds such as 2-bromoacetophenone commonly used in the industry.

Method for synthesizing novel imidazole pyranone compounds containing chalcogens

The invention discloses a method for synthesizing novel imidazole pyranone compounds containing chalcogens. The method comprises the steps as follows: firstly, 4-hydroxycoumarin compounds and triflicanhydride react, and 4-triflate-based coumarins are gene