8-Bromo-4-methyl-quinoline 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 8-position and a methyl group at the 4-position contributes to its unique chemical properties. This compound typically exhibits a pale yellow to brownish color and is soluble in organic solvents. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The bromine substituent can enhance reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the methyl group can influence the compound's electronic properties and steric hindrance, affecting its interaction with biological targets. As with many halogenated compounds, safety precautions should be taken when handling 8-bromo-4-methyl-quinoline, as it may pose environmental and health risks. Overall, this compound is of interest in both synthetic organic chemistry and drug discovery.

8-bromo-4-methyl-quinoline

172939-50-3: 8-Bromo-4-methyl-quinoline 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 8-position and a methyl group at the 4-position contributes to its unique chemical properties. This compound typically exhibits a pale yellow to brownish color and is soluble in organic solvents. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The bromine substituent can enhance reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the methyl group can influence the compound's electronic properties and steric hindrance, affecting its interaction with biological targets. As with many halogenated compounds, safety precautions should be taken when handling 8-bromo-4-methyl-quinoline, as it may pose environmental and health risks. Overall, this compound is of interest in both synthetic organic chemistry and drug discovery.

CAS 172939-50-3

8-bromo-4-methyl-quinoline

8-Bromo-4-methylquinoline

Ref: IN-DA007C0G

8-Bromo-4-methylquinoline

Ref: 54-OR92660

8-Bromo-4-methylquinoline

Ref: 10-F639867