4-(Chloromethyl)quinoline is an organic compound characterized by a quinoline backbone with a chloromethyl group attached at the 4-position. This compound typically appears as a yellow to brown solid and is known for its aromatic properties due to the presence of the quinoline structure, which consists of a fused benzene and pyridine ring. It is moderately soluble in organic solvents like ethanol and dichloromethane but has limited solubility in water. The chloromethyl group introduces reactivity, making it a useful intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The compound may exhibit biological activity, including antimicrobial or antitumor properties, which is common among quinoline derivatives. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Proper storage in a cool, dry place away from light is recommended to maintain its stability. Overall, 4-(Chloromethyl)quinoline serves as an important building block in various chemical applications.

4-(Chloromethyl)quinoline

5632-17-7: 4-(Chloromethyl)quinoline, Lepidine, α-chloro-, 4-Chloromethylquinoline, Quinoline, 4-(chloromethyl)-

4-Chloromethyl-Quinoline

4-Chloromethylquinoline is a chemical compound that belongs to the class of naphthalenes. It has been shown to form carbanion, metallacycles, and chloride isomers. 4-Chloromethylquinoline has two stereoisomers, which can be differentiated by the size of their cavity. The larger cavity isomer has been shown to be more stable and selective than the smaller cavity isomer. This compound can be used as a ligand for optimization or for advances in chemistry.

CAS 5632-17-7: 4-(Chloromethyl)quinoline

4-Chloromethyl-Quinoline

Ref: 54-OR1011512

4-Chloromethylquinoline

Ref: 3D-FC43137

4-Chloromethylquinoline

Ref: IN-DA00EK08