31562-99-9

Basic information

• Product Name: 4-IMIDAZO[1,2-A]PYRIDIN-2-YLPHENYL METHYL ETHER
• Synonyms: 2-(4-METHOXY-PHENYL)-IMIDAZO[1,2-A]PYRIDINE;4-IMIDAZO[1,2-A]PYRIDIN-2-YLPHENYL METHYL ETHER
• CAS NO: 31562-99-9
• Molecular Formula: C₁₄H₁₂N₂O
• Molecular Weight: 224.26
• Mol File: 31562-99-9.mol
• Article Data: 98

Chemical Properties

• Melting Point: 133-134 °C
• Appearance: /
• Density: 1.15±0.1 g/cm3(Predicted)
• PKA: 6.99±0.50(Predicted)
• CAS DataBase Reference: 4-IMIDAZO[1,2-A]PYRIDIN-2-YLPHENYL METHYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: 4-IMIDAZO[1,2-A]PYRIDIN-2-YLPHENYL METHYL ETHER(31562-99-9)
• EPA Substance Registry System: 4-IMIDAZO[1,2-A]PYRIDIN-2-YLPHENYL METHYL ETHER(31562-99-9)

Safety Data

• Hazardous Substances Data: 31562-99-9(Hazardous Substances Data)

Usage

General Description

4-IMIDAZO[1,2-A]PYRIDIN-2-YLPHENYL METHYL ETHER is a chemical compound with the molecular formula C16H13N3O and a molecular weight of 263.29 g/mol. It is a phenyl methyl ether derivative containing an imidazo[1,2-a]pyridine moiety. 4-IMIDAZO[1,2-A]PYRIDIN-2-YLPHENYL METHYL ETHER is typically used in organic synthesis and medicinal chemistry as a building block for the synthesis of various biologically active compounds. It may also have potential pharmaceutical applications due to its structural features and interactions with biological targets. However, further research is needed to fully understand its properties and potential uses.

Upstream product

• 54187-96-1 1-(chloromethyl)-1H-benzotriazole 
• 110-86-1 pyridine 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 504-29-0 2-aminopyridine 
• 768-60-5 4-methoxyphenylacetylen 
• 32117-52-5 1-(1-(4-methoxyphenyl)ethylidene)-2-tosylhydrazine 
• 1515-95-3 p-ethylanisole 
• 70-11-1 α-bromoacetophenone 
• 2475-92-5 4-methoxyacetophenone oxime 
• 96155-57-6 1-(4-methoxyphenyl)ethanone O-acetyl oxime 
• 2196-99-8 2-chloro-1-(4-methoxyphenyl)ethanone 
• 637-69-4 4-Methoxystyrene 
• 80336-72-7 2-iodo-1-(4-methoxyphenyl)ethanone 
• 75-52-5 nitromethane 

Downstream Products

• 324741-47-1 2-(4-methoxyphenyl)-3-phenylimidazo[1,2-a]pyridine 
• 1353511-89-3 C₂₀H₁₅N₃O₃ 
• 1176664-83-7 (2-(4-methoxyphenyl)imidazo[1,2-a]pyridin-3-yl)methanol 
• 1417910-26-9 C₁₅H₁₃N₅O 
• 1417910-44-1 2-(4-methoxyphenyl)-3-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)-1H-imidazo[1,2-a]pyridine 
• 1417910-46-3 3-((4-(4-fluorophenyl)-1H-1,2,3-triazol-1-yl)methyl)-2-(4-methoxyphenyl)-1H-imidazo[1,2-a]pyridine 
• 426239-77-2 2-(4-methoxyphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde 

Relevant articles and documents

Hypervalent Iodine in Synthesis. 94. A Facile Synthesis of 2-Substituted-imidazo[1,2-a]pyridines by Cyclocondensation of Alkynyl(phenyl) iodonium Salts and 2-Aminopyridine

A facile method for the synthesis of 2-substituted-imidazo[1,2-a]pyridines is achieved by cyclocondensation of alkynyl(phenyl)iodonium salts with 2-aminopyridine.

Eucalyptol: A new solvent for the synthesis of heterocycles containing oxygen, sulfur and nitrogen

We report here the first investigation of the use of eucalyptol as a new solvent for organic transformations. Heterocycles containing oxygen, sulfur and nitrogen were chosen as targets or as starting materials for widely used palladium-catalysed cross-cou

Solvent and catalyst-free synthesis of imidazo[1,2-a]pyridines by grindstone chemistry

The present work describes the solvent and catalyst-free synthesis of imidazo[1,2-a]pyridines in excellent to nearly quantitative yields from 2-aminopyridines and a wide variety of ω-bromomethylketones using a grindstone procedure at 25°C to 30°C for 3 to

Micellar Catalysis: Visible-Light Mediated Imidazo[1,2-a]pyridine C—H Amination with N-Aminopyridinium Salt Accelerated by Surfactant in Water

A light-promoted metal-free protocol for the amination of imidazo[1,2-a]pyridines with N-aminopyridinium salt by the assistance of surfactants in water was reported, charactering mild and environmentally benign conditions, as well as great functional grou