3-Bromoimidazo[1,2-a]pyridin-8-amine 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 of the imidazole ring enhances its reactivity and can influence its biological activity. The amino group at the 8-position serves as a potential site for further chemical modifications, making it a versatile building block in medicinal chemistry. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group. Its structure suggests potential applications in pharmaceuticals, particularly in the development of compounds targeting various biological pathways. Additionally, the bromine substituent can facilitate reactions such as nucleophilic substitutions or coupling reactions, which are valuable in synthetic organic chemistry. Overall, 3-bromoimidazo[1,2-a]pyridin-8-amine is of interest for its potential applications in drug discovery and development.

3-bromoimidazo[1,2-a]pyridin-8-amine

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3-Bromoimidazo[1,2-a]pyridin-8-amine

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CAS 1232431-81-0: 3-bromoimidazo[1,2-a]pyridin-8-amine

3-Bromoimidazo[1,2-a]pyridin-8-amine

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Imidazo[1,2-a]pyridin-8-amine, 3-bromo-

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3-Bromoimidazo[1,2-a]pyridin-8-amine

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