5-Bromo-2-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 5-position and a methoxy group at the 2-position contributes to its unique chemical properties. This compound typically appears as a solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. It may exhibit antimicrobial, anti-inflammatory, or anticancer properties, making it of interest in drug discovery. The bromine substituent can enhance the compound's reactivity and influence its interaction with biological targets. Additionally, the methoxy group can affect the solubility and stability of the compound in various solvents. As with many quinoline derivatives, 5-Bromo-2-methoxyquinoline may also participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it a versatile building block in organic synthesis. Safety and handling precautions should be observed due to the potential toxicity of brominated compounds.

5-Bromo-2-methoxyquinoline

99455-06-8: 5-Bromo-2-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 5-position and a methoxy group at the 2-position contributes to its unique chemical properties. This compound typically appears as a solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. It may exhibit antimicrobial, anti-inflammatory, or anticancer properties, making it of interest in drug discovery. The bromine substituent can enhance the compound's reactivity and influence its interaction with biological targets. Additionally, the methoxy group can affect the solubility and stability of the compound in various solvents. As with many quinoline derivatives, 5-Bromo-2-methoxyquinoline may also participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it a versatile building block in organic synthesis. Safety and handling precautions should be observed due to the potential toxicity of brominated compounds.

CAS 99455-06-8

5-Bromo-2-methoxyquinoline

Quinoline, 5-bromo-2-methoxy-

Ref: IN-DA00IKAF

5-Bromo-2-methoxyquinoline

Ref: 54-OR80106

5-Bromo-2-methoxyquinoline

Ref: 10-F910224