6-Bromo-4-chloro-1H-imidazo[4,5-c]pyridine is a heterocyclic compound characterized by its fused imidazole and pyridine rings, which contribute to its unique chemical properties. The presence of bromine and chlorine substituents at the 6 and 4 positions, respectively, enhances its reactivity and potential for various chemical transformations. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with imidazo-pyridine derivatives. The compound may also participate in various reactions such as nucleophilic substitutions or coupling reactions, making it a valuable intermediate in synthetic organic chemistry. Additionally, its specific electronic and steric properties can influence its interactions with biological targets, which is of interest in drug design and discovery. Safety and handling precautions should be observed, as with many halogenated compounds, due to potential toxicity and environmental concerns.

6-bromo-4-chloro-1H-imidazo[4,5-c]pyridine

1638767-93-7: 6-Bromo-4-chloro-1H-imidazo[4,5-c]pyridine is a heterocyclic compound characterized by its fused imidazole and pyridine rings, which contribute to its unique chemical properties. The presence of bromine and chlorine substituents at the 6 and 4 positions, respectively, enhances its reactivity and potential for various chemical transformations. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with imidazo-pyridine derivatives. The compound may also participate in various reactions such as nucleophilic substitutions or coupling reactions, making it a valuable intermediate in synthetic organic chemistry. Additionally, its specific electronic and steric properties can influence its interactions with biological targets, which is of interest in drug design and discovery. Safety and handling precautions should be observed, as with many halogenated compounds, due to potential toxicity and environmental concerns.

CAS 1638767-93-7

6-bromo-4-chloro-1H-imidazo[4,5-c]pyridine

3H-Imidazo[4,5-c]pyridine, 6-bromo-4-chloro-

Ref: IN-DA001UHR

6-BROMO-4-CHLORO-1H-IMIDAZO[4,5-C]PYRIDINE

Ref: 10-F474148