Imidazo[1,2-a]pyridine-8-methanol is a heterocyclic organic compound characterized by its fused imidazole and pyridine rings, which contribute to its unique chemical properties. The presence of a hydroxymethyl group (-CH2OH) at the 8-position enhances its reactivity and solubility in polar solvents. This compound typically exhibits moderate to high polarity due to the hydroxyl group, making it suitable for various chemical reactions, including nucleophilic substitutions and condensation reactions. Its structure allows for potential interactions with biological targets, which has led to interest in its pharmacological properties. Imidazo[1,2-a]pyridine derivatives are often studied for their potential as therapeutic agents, particularly in the fields of oncology and neurology. The compound's stability, reactivity, and ability to form hydrogen bonds are significant factors in its applications in medicinal chemistry. As with many heterocycles, the electronic properties of the nitrogen atoms in the rings can influence its behavior in chemical reactions and interactions with other molecules.

IMidazo[1,2-a]pyridine-8-Methanol

111477-17-9: Imidazo[1,2-a]pyridine-8-methanol is a heterocyclic organic compound characterized by its fused imidazole and pyridine rings, which contribute to its unique chemical properties. The presence of a hydroxymethyl group (-CH2OH) at the 8-position enhances its reactivity and solubility in polar solvents. This compound typically exhibits moderate to high polarity due to the hydroxyl group, making it suitable for various chemical reactions, including nucleophilic substitutions and condensation reactions. Its structure allows for potential interactions with biological targets, which has led to interest in its pharmacological properties. Imidazo[1,2-a]pyridine derivatives are often studied for their potential as therapeutic agents, particularly in the fields of oncology and neurology. The compound's stability, reactivity, and ability to form hydrogen bonds are significant factors in its applications in medicinal chemistry. As with many heterocycles, the electronic properties of the nitrogen atoms in the rings can influence its behavior in chemical reactions and interactions with other molecules.

Imidazo[1,2-a]pyridin-8-ylmethanol

<p>Imidazo[1,2-a]pyridin-8-ylmethanol</p>

CAS 111477-17-9

IMidazo[1,2-a]pyridine-8-Methanol

Imidazo[1,2-a]pyridin-8-ylmethanol

Ref: IN-DA007SVT

Imidazo[1,2-a]pyridin-8-ylmethanol

Ref: 54-OR305170

Imidazo[1,2-a]pyridin-8-ylmethanol

Ref: 10-F230186