Imidazo[1,2-a]pyridine, 5-chloro-7-methyl- is a heterocyclic organic compound characterized by its fused imidazole and pyridine rings. This compound features a chlorine atom at the 5-position and a methyl group at the 7-position of the imidazo[1,2-a]pyridine structure, which contributes to its unique chemical properties. It is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. The presence of the chlorine and methyl substituents can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. This compound may also exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its molecular structure allows for potential interactions with biological targets, which can be explored in pharmacological studies. As with many heterocycles, it may also participate in coordination chemistry, forming complexes with metal ions. Overall, imidazo[1,2-a]pyridine derivatives are valuable in both synthetic and medicinal chemistry contexts.

IMidazo[1,2-a]pyridine, 5-chloro-7-Methyl-

442127-23-3: Imidazo[1,2-a]pyridine, 5-chloro-7-methyl- is a heterocyclic organic compound characterized by its fused imidazole and pyridine rings. This compound features a chlorine atom at the 5-position and a methyl group at the 7-position of the imidazo[1,2-a]pyridine structure, which contributes to its unique chemical properties. It is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. The presence of the chlorine and methyl substituents can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. This compound may also exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its molecular structure allows for potential interactions with biological targets, which can be explored in pharmacological studies. As with many heterocycles, it may also participate in coordination chemistry, forming complexes with metal ions. Overall, imidazo[1,2-a]pyridine derivatives are valuable in both synthetic and medicinal chemistry contexts.

CAS 442127-23-3

IMidazo[1,2-a]pyridine, 5-chloro-7-Methyl-

5-Chloro-7-Methylimidazo[1,2-A]Pyridine

Ref: IN-DA00I8E8

5-CHLORO-7-METHYLIMIDAZO[1,2-A]PYRIDINE

Ref: 10-F469383