8-Chloro-5-methylquinoline is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a chlorine atom at the 8-position and a methyl group at the 5-position contributes to its unique chemical properties. This compound typically appears as a yellow to brown solid and is known for its potential applications in pharmaceuticals, particularly as an intermediate in the synthesis of various bioactive molecules. It exhibits moderate solubility in organic solvents, while its solubility in water is limited. The compound may also display biological activity, making it of interest in medicinal chemistry. Its reactivity can be influenced by the electron-withdrawing nature of the chlorine atom, which can affect its electrophilic and nucleophilic behavior. Safety data indicates that, like many chlorinated compounds, it should be handled with care due to potential toxicity and environmental concerns. Overall, 8-Chloro-5-methylquinoline is a significant compound in organic synthesis and medicinal chemistry research.

8-Chloro-5-methylquinoline

56961-81-0: Quinoline, 8-chloro-5-methyl-, T66 Bnj G1 Jg [Wln], 8-Chloro-5-methylquinoline

8-Chloro-5-methylquinoline (8C8MQ) is a heteroaryl compound that can be used for dehalogenation. 8C8MQ has been shown to convert bromobenzene to the corresponding benzene derivative in a coupling reaction with lithium chloride. It is also an important chemical intermediate for the synthesis of other heteroaryl compounds. 8C8MQ can be synthesized by reacting methyl iodide and 8-chloroquinoline in the presence of lithium and dimethylformamide as solvent. The reaction can be monitored by spectroscopy, which will show that the product is a dimer.

CAS 56961-81-0: 8-Chloro-5-methylquinoline

8-Chloro-5-methylquinoline

Ref: 3D-FC153111

8-CHLORO-5-METHYLQUINOLINE

Ref: IN-DA00E9RV