89192-94-9

Basic information

• Product Name: Imidazo[1,2-a]pyridine, 3-methoxy-2-phenyl-
• CAS NO: 89192-94-9
• Molecular Formula: C14H12N2O
• Molecular Weight: 224.262
• Mol File: 89192-94-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Imidazo[1,2-a]pyridine, 3-methoxy-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Imidazo[1,2-a]pyridine, 3-methoxy-2-phenyl-(89192-94-9)
• EPA Substance Registry System: Imidazo[1,2-a]pyridine, 3-methoxy-2-phenyl-(89192-94-9)

Safety Data

• Hazardous Substances Data: 89192-94-9(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 4105-21-9 2-phenylimidazo[1,2-a]pyridine 
• 504-29-0 2-aminopyridine 
• 4079-52-1 methoxymethyl phenyl ketone 
• 25142-28-3 2-phenyl-1H-imidazo<1,2-a>pyridinium-3-olate 
• 74-88-4 methyl iodide 

Downstream Products

• 89193-05-5 5,8-Dimethyl-3-methoxy-2-phenylimidazo<1,2-a>pyridine 

Relevant articles and documents

I2-mediated and direct synthesis of 3-phenoxy imidazo heterocycles

An I2-mediated protocol was proposed for the synthesis of 3-phenoxy imidazo heterocycles from aromatic ketones and 2-aminopyridines or 2-aminobenzothiazole. This direct, efficient and operationally simple method provided a fundamentally novel a

Visible Light Organic Photoredox-Catalyzed C-H Alkoxylation of Imidazopyridine with Alcohol

The visible light-mediated C-3 alkoxylation of imidazopyridines with alcohols has been achieved using rose bengal as an organic photoredox catalyst at room temperature. Widely abundant air acts as the terminal oxidant that avoids the use of a stoichiometric amount of peroxo compounds. A wide range of functional groups could be tolerated under the reaction conditions to produce C(sp2)-H alkoxylated products in high yields.

The Directed Lithiation of 3-Methoxy-2-phenylimidazopyridine

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