6-Bromo-4-methoxyquinoline is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 6-position and a methoxy group at the 4-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents, reflecting its aromatic nature. It may display biological activity, making it of interest in medicinal chemistry and drug development. The bromine substituent can enhance reactivity in electrophilic substitution reactions, while the methoxy group can influence the compound's electronic properties and steric hindrance. Additionally, 6-bromo-4-methoxyquinoline may exhibit fluorescence, which can be useful in various analytical applications. Its CAS number, 874792-20-8, allows for precise identification in chemical databases. Overall, this compound's structural features suggest potential applications in pharmaceuticals, agrochemicals, and materials science, warranting further investigation into its reactivity and biological activity.

6-bromo-4-methoxyquinoline

874792-20-8: 6-Bromo-4-methoxyquinoline is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 6-position and a methoxy group at the 4-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents, reflecting its aromatic nature. It may display biological activity, making it of interest in medicinal chemistry and drug development. The bromine substituent can enhance reactivity in electrophilic substitution reactions, while the methoxy group can influence the compound's electronic properties and steric hindrance. Additionally, 6-bromo-4-methoxyquinoline may exhibit fluorescence, which can be useful in various analytical applications. Its CAS number, 874792-20-8, allows for precise identification in chemical databases. Overall, this compound's structural features suggest potential applications in pharmaceuticals, agrochemicals, and materials science, warranting further investigation into its reactivity and biological activity.

CAS 874792-20-8

6-bromo-4-methoxyquinoline

6-Bromo-4-methoxyquinoline

Ref: IN-DA004EPA

6-Bromo-4-methoxyquinoline

Ref: 54-OR16166

6-Bromo-4-methoxyquinoline

Ref: 10-F092180