4-(Chloromethyl)-2-methylquinoline is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a chloromethyl group at the 4-position and a methyl group at the 2-position contributes to its unique chemical properties. This compound typically appears as a yellow to brown solid and is soluble in organic solvents. It may exhibit biological activity, making it of interest in medicinal chemistry and drug development. The chloromethyl group can participate in nucleophilic substitution reactions, allowing for further functionalization. Additionally, the quinoline moiety is known for its potential applications in pharmaceuticals, agrochemicals, and as a fluorescent probe. Safety data indicates that, like many chlorinated compounds, it should be handled with care due to potential toxicity and environmental concerns. Overall, 4-(chloromethyl)-2-methylquinoline is a versatile compound with significant implications in various chemical research fields.

4-(chloromethyl)-2-methylquinoline

288399-19-9: Quinoline, 4-(chloromethyl)-2-methyl-, 4-(Chloromethyl)-2-methylquinoline

Quinoline, 4-(chloromethyl)-2-methyl-

4-Chloromethyl-2-methylquinoline

4-(Chloromethyl)-2-methylquinoline is a hydroxamic acid that inhibits the activity of a number of enzymes, including isomerases and proteases. It has been shown to be an inhibitor of tnf-α and isomers. 4-(Chloromethyl)-2-methylquinoline binds to the subunit II of the enzyme protein kinase C, which may lead to its therapeutic effect against inflammation.

CAS 288399-19-9: 4-(chloromethyl)-2-methylquinoline

Quinoline, 4-(chloromethyl)-2-methyl-

Ref: IN-DA002WQZ

4-Chloromethyl-2-methylquinoline

Ref: 10-F036022

4-(Chloromethyl)-2-methylquinoline

Ref: 3D-FC148794

4-(Chloromethyl)-2-methylquinoline

Ref: 54-OR16603