3-Bromo-6-methylH-imidazo[1,2-a]pyridine is a heterocyclic organic compound characterized by its fused imidazole and pyridine rings, which contribute to its unique chemical properties. The presence of a bromine atom at the 3-position and a methyl group at the 6-position enhances its reactivity and solubility in various organic solvents. This compound typically exhibits a pale yellow to brownish appearance and is known for its potential biological activity, making it of interest in medicinal chemistry and drug development. Its structure allows for various interactions, including hydrogen bonding and π-π stacking, which can influence its behavior in biological systems. The compound's CAS number, 866135-71-9, is a unique identifier that facilitates its identification in chemical databases. Due to its specific functional groups, it may participate in electrophilic substitution reactions and can serve as a precursor for further chemical modifications. Overall, 3-bromo-6-methylH-imidazo[1,2-a]pyridine is a versatile compound with applications in research and potential therapeutic uses.

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

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3-Bromo-6-methylimidazo[1,2-a]pyridine

3-BROMO-6-METHYLIMIDAZO[1,2-A]PYRIDINE

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CAS 866135-71-9: 3-bromo-6-methylH-imidazo[1,2-a]pyridine

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