3-Bromoimidazo[1,2-a]pyridine-7-carbonitrile is a heterocyclic organic compound characterized by its imidazole and pyridine rings, which contribute to its unique chemical properties. The presence of a bromine atom at the 3-position and a cyano group at the 7-position enhances its reactivity and potential applications in medicinal chemistry and material science. This compound typically exhibits a solid state at room temperature and is soluble in polar organic solvents. Its structure allows for various interactions, making it a candidate for further functionalization or as a building block in the synthesis of more complex molecules. The compound may also display biological activity, which is of interest in drug discovery and development. As with many heterocycles, it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the electron-rich nature of the nitrogen atoms in the rings. Safety and handling precautions should be observed, as with all brominated compounds, due to potential toxicity and environmental concerns.

3-bromoimidazo[1,2-a]pyridine-7-carbonitrile

1392210-94-4: 3-Bromoimidazo[1,2-a]pyridine-7-carbonitrile is a heterocyclic organic compound characterized by its imidazole and pyridine rings, which contribute to its unique chemical properties. The presence of a bromine atom at the 3-position and a cyano group at the 7-position enhances its reactivity and potential applications in medicinal chemistry and material science. This compound typically exhibits a solid state at room temperature and is soluble in polar organic solvents. Its structure allows for various interactions, making it a candidate for further functionalization or as a building block in the synthesis of more complex molecules. The compound may also display biological activity, which is of interest in drug discovery and development. As with many heterocycles, it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the electron-rich nature of the nitrogen atoms in the rings. Safety and handling precautions should be observed, as with all brominated compounds, due to potential toxicity and environmental concerns.

3-Bromoimidazo[1,2-a]pyridine-7-carbonitrile

CAS 1392210-94-4

3-bromoimidazo[1,2-a]pyridine-7-carbonitrile

3-Bromoimidazo[1,2-a]pyridine-7-carbonitrile

Ref: 54-OR83106

3-Bromoimidazo[1,2-a]pyridine-7-carbonitrile

Ref: 10-F720031