6-MethylH-imidazo[1,2-a]pyridine-3-carbaldehyde is a heterocyclic organic compound characterized by its imidazo-pyridine structure, which incorporates both nitrogen and carbon atoms in its ring system. This compound features a methyl group at the 6-position and an aldehyde functional group at the 3-position, contributing to its reactivity and potential applications in organic synthesis. The presence of the imidazole ring imparts unique electronic properties, making it of interest in medicinal chemistry and material science. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its chemical behavior can be influenced by the aldehyde group, which can participate in various reactions, such as condensation and oxidation. Additionally, the compound's structure suggests potential biological activity, which may warrant further investigation in pharmacological studies. As with many heterocycles, it may also serve as a building block for more complex molecules in synthetic chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.

6-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde

933752-89-7: 6-MethylH-imidazo[1,2-a]pyridine-3-carbaldehyde is a heterocyclic organic compound characterized by its imidazo-pyridine structure, which incorporates both nitrogen and carbon atoms in its ring system. This compound features a methyl group at the 6-position and an aldehyde functional group at the 3-position, contributing to its reactivity and potential applications in organic synthesis. The presence of the imidazole ring imparts unique electronic properties, making it of interest in medicinal chemistry and material science. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its chemical behavior can be influenced by the aldehyde group, which can participate in various reactions, such as condensation and oxidation. Additionally, the compound's structure suggests potential biological activity, which may warrant further investigation in pharmacological studies. As with many heterocycles, it may also serve as a building block for more complex molecules in synthetic chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.

CAS 933752-89-7

6-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde

6-Methylimidazo[1,2-a]pyridine-3-carbaldehyde

Ref: IN-DA0063OE

6-Methylimidazo[1,2-a]pyridine-3-carbaldehyde

Ref: 54-OR909922

6-Methylimidazo[1,2-a]pyridine-3-carbaldehyde

Ref: 10-F209269