4-Bromo-6-methoxy-2-methylquinoline is a chemical compound belonging to the quinoline family, characterized by a bicyclic structure that includes a benzene ring fused to a pyridine ring. This compound features a bromine atom at the 4-position, a methoxy group (-OCH3) at the 6-position, and a methyl group (-CH3) at the 2-position of the quinoline ring. The presence of these substituents influences its chemical reactivity and physical properties, such as solubility and boiling point. Typically, compounds like this exhibit biological activity, making them of interest in medicinal chemistry and drug development. The bromine atom can enhance the compound's reactivity, while the methoxy group may contribute to its lipophilicity, potentially affecting its interaction with biological targets. Additionally, the molecular structure suggests that it may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, which are common in aromatic compounds. Overall, 4-bromo-6-methoxy-2-methylquinoline is a versatile compound with potential applications in pharmaceuticals and organic synthesis.

4-bromo-6-methoxy-2-methylquinoline

856095-00-6: 4-Bromo-6-methoxy-2-methylquinoline is a chemical compound belonging to the quinoline family, characterized by a bicyclic structure that includes a benzene ring fused to a pyridine ring. This compound features a bromine atom at the 4-position, a methoxy group (-OCH3) at the 6-position, and a methyl group (-CH3) at the 2-position of the quinoline ring. The presence of these substituents influences its chemical reactivity and physical properties, such as solubility and boiling point. Typically, compounds like this exhibit biological activity, making them of interest in medicinal chemistry and drug development. The bromine atom can enhance the compound's reactivity, while the methoxy group may contribute to its lipophilicity, potentially affecting its interaction with biological targets. Additionally, the molecular structure suggests that it may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, which are common in aromatic compounds. Overall, 4-bromo-6-methoxy-2-methylquinoline is a versatile compound with potential applications in pharmaceuticals and organic synthesis.

4-Bromo-6-methoxy-2-methylquinoline

<p>4-Bromo-6-methoxy-2-methylquinoline</p>

CAS 856095-00-6

4-bromo-6-methoxy-2-methylquinoline

4-Bromo-6-methoxy-2-methylquinoline

Ref: IN-DA008HA7

4-Bromo-6-methoxy-2-methylquinoline

Ref: 54-OR309244

4-Bromo-6-methoxy-2-methylquinoline

Ref: 10-F318316