2-(4-Fluoro-phenyl)-7-methyl-imidazo[1,2-a]pyridine is a heterocyclic organic compound characterized by its complex structure, which includes an imidazo[1,2-a]pyridine core substituted with a 4-fluorophenyl group and a methyl group at specific positions. This compound typically exhibits properties such as moderate to high lipophilicity due to the presence of aromatic rings, which can influence its solubility and bioavailability. The fluorine atom in the 4-position of the phenyl ring can enhance the compound's metabolic stability and may affect its interaction with biological targets. Additionally, the imidazo[1,2-a]pyridine framework is known for its potential pharmacological activities, including anti-inflammatory and anticancer properties. The compound's molecular structure allows for various interactions, making it a subject of interest in medicinal chemistry and drug development. Its specific reactivity and stability can be influenced by the electronic effects of the substituents, making it a valuable candidate for further research in therapeutic applications.

2-(4-FLUORO-PHENYL)-7-METHYL-IMIDAZO[1,2-A]PYRIDINE

378766-08-6: 2-(4-Fluoro-phenyl)-7-methyl-imidazo[1,2-a]pyridine is a heterocyclic organic compound characterized by its complex structure, which includes an imidazo[1,2-a]pyridine core substituted with a 4-fluorophenyl group and a methyl group at specific positions. This compound typically exhibits properties such as moderate to high lipophilicity due to the presence of aromatic rings, which can influence its solubility and bioavailability. The fluorine atom in the 4-position of the phenyl ring can enhance the compound's metabolic stability and may affect its interaction with biological targets. Additionally, the imidazo[1,2-a]pyridine framework is known for its potential pharmacological activities, including anti-inflammatory and anticancer properties. The compound's molecular structure allows for various interactions, making it a subject of interest in medicinal chemistry and drug development. Its specific reactivity and stability can be influenced by the electronic effects of the substituents, making it a valuable candidate for further research in therapeutic applications.

2-(4-Fluorophenyl)-7-methylimidazo[1,2-a]pyridine

<p>2-(4-Fluorophenyl)-7-methylimidazo[1,2-a]pyridine</p>

CAS 378766-08-6

2-(4-FLUORO-PHENYL)-7-METHYL-IMIDAZO[1,2-A]PYRIDINE

2-(4-Fluorophenyl)-7-methylimidazo[1,2-a]pyridine

Ref: IN-DA0077GN

2-(4-Fluorophenyl)-7-methylimidazo[1,2-a]pyridine

Ref: 54-PC1001271

2-(4-Fluorophenyl)-7-methylimidazo[1,2-a]pyridine

Ref: 3D-DQA76608