2-(4-Bromo-1H-imidazol-1-yl)pyridine is a chemical compound characterized by its unique structure, which includes a pyridine ring substituted with a 4-bromo-1H-imidazole moiety. This compound typically exhibits properties associated with both heterocyclic aromatic compounds and halogenated derivatives. The presence of the bromine atom introduces notable reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The imidazole ring contributes to its biological activity, as imidazole derivatives are often found in pharmaceuticals and agrochemicals. Additionally, the compound may exhibit moderate to high solubility in polar organic solvents, while its solid-state properties can vary based on crystallization conditions. Its molecular interactions may be influenced by hydrogen bonding and π-π stacking due to the aromatic nature of both the pyridine and imidazole rings. Overall, 2-(4-bromo-1H-imidazol-1-yl)pyridine is of interest in medicinal chemistry and materials science due to its potential applications in drug development and as a building block in organic synthesis.

2-(4-BROMO-1H-IMIDAZOL-1-YL)PYRIDINE

556775-77-0: 2-(4-Bromo-1H-imidazol-1-yl)pyridine is a chemical compound characterized by its unique structure, which includes a pyridine ring substituted with a 4-bromo-1H-imidazole moiety. This compound typically exhibits properties associated with both heterocyclic aromatic compounds and halogenated derivatives. The presence of the bromine atom introduces notable reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The imidazole ring contributes to its biological activity, as imidazole derivatives are often found in pharmaceuticals and agrochemicals. Additionally, the compound may exhibit moderate to high solubility in polar organic solvents, while its solid-state properties can vary based on crystallization conditions. Its molecular interactions may be influenced by hydrogen bonding and π-π stacking due to the aromatic nature of both the pyridine and imidazole rings. Overall, 2-(4-bromo-1H-imidazol-1-yl)pyridine is of interest in medicinal chemistry and materials science due to its potential applications in drug development and as a building block in organic synthesis.

CAS 556775-77-0

2-(4-BROMO-1H-IMIDAZOL-1-YL)PYRIDINE

2-(4-Bromo-1H-imidazol-1-yl)pyridine

Ref: 10-F240155