2-Chloro-4,8-dimethylquinoline is an organic compound belonging to the quinoline family, characterized by a bicyclic structure that includes a benzene ring fused to a pyridine ring. This compound features a chlorine atom at the second position and two methyl groups at the fourth and eighth positions of the quinoline ring. It is typically a yellow to brown solid at room temperature and is sparingly soluble in water but more soluble in organic solvents such as ethanol and acetone. The presence of the chlorine atom and methyl groups influences its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. 2-Chloro-4,8-dimethylquinoline may exhibit biological activity, making it of interest for research in medicinal chemistry. As with many organic compounds, proper handling and safety precautions are essential due to potential toxicity and environmental impact.

2-Chloro-4,8-dimethylquinoline

3913-17-5: Quinoline, 2-Chloro-4,8-Dimethyl-

2-Chloro-4,8-dimethylquinoline is a synthetic drug that inhibits the synthesis of single-stranded DNA. It also binds to ethylene and forms a heterocycle with two boron atoms in the molecule. This drug has been shown to be effective against cancer cells in vitro and in vivo. It can be used for the treatment of leukemia, lymphoma, and myeloma. 2-Chloro-4,8-dimethylquinoline was synthesized by dehydrogenation of an ethylenethioether with diborane followed by reaction with an anion from solvents such as dichloromethane or acetone. The compound is synthesized using a synthetic pathway that begins with the reaction between ethylene and diborane.

CAS 3913-17-5: 2-Chloro-4,8-dimethylquinoline

2-Chloro-4,8-dimethylquinoline

Ref: 3D-FC42177

2-Chloro-4,8-dimethylquinoline

Ref: 10-F092548

2-Chloro-4,8-dimethylquinoline

Ref: 54-OR931562

2-Chloro-4,8-dimethylquinoline

Ref: IN-DA0076HY