5-Chloroquinaldine is an organic compound characterized by its structure, which consists of a quinoline ring substituted with a chlorine atom at the 5-position and a methyl group at the 2-position. It is typically a pale yellow to brown solid with a distinct aromatic odor. This compound is known for its applications in the synthesis of various pharmaceuticals and agrochemicals, owing to its biological activity and ability to act as an intermediate in chemical reactions. 5-Chloroquinaldine exhibits moderate solubility in organic solvents, while its solubility in water is limited. The presence of the chlorine atom enhances its reactivity, making it a valuable building block in organic synthesis. Additionally, it may exhibit antimicrobial properties, which can be explored in medicinal chemistry. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity and environmental impact.

5-Chloroquinaldine

5-Chloro-2-methylquinoline

5-Chloro-2-methyl-quinoline is a molecule that irreversibly inhibits cancer cell growth. It has potent anticancer effects and shows activity against human leukemia HL60 cells as well as lemongrass oil, which is an antimicrobial agent. 5-Chloro-2-methyl-quinoline also shows redox potentials that are similar to those of the amino acid methionine and can be degraded by protein synthesis. This molecule also participates in signal pathways such as the MAP kinase pathway, which may lead to its anticancer effects. 5-Chloro-2-methyl-quinoline can undergo Friedel-Crafts reactions with a number of organic compounds, including benzene and acetic anhydride to form 2,4,5-trichlorobenzophenone or chloropicrin.

CAS 4964-69-6: 5-Chloroquinaldine

5-Chloro-2-methylquinoline

Ref: 10-F239090

5-Chloroquinaldine

Ref: 54-OR51848

5-Chloro-2-methyl-quinoline

Ref: 3D-FC33088

5-Chloroquinaldine

Ref: IN-DA00DEB8