2,3-Dichloroquinoline is a chemical compound characterized by its bicyclic structure, which consists of a quinoline core with two chlorine substituents at the 2 and 3 positions. This compound is typically a pale yellow to brown solid at room temperature and is known for its aromatic properties due to the presence of the quinoline ring system. It is moderately soluble in organic solvents but has limited solubility in water. 2,3-Dichloroquinoline exhibits biological activity, making it of interest in medicinal chemistry and research, particularly for its potential applications in pharmaceuticals. The presence of chlorine atoms enhances its reactivity and can influence its interaction with biological targets. As with many chlorinated compounds, it is important to handle 2,3-dichloroquinoline with care due to potential toxicity and environmental concerns. Proper safety measures should be taken when working with this substance, including the use of personal protective equipment and adherence to relevant regulations regarding hazardous materials.

2,3-dichloroquinoline

2,3-Dichloroquinoline

2,3-Dichloroquinoline is a dichloroquinoline that has been shown to have anti-inflammatory properties. It may be used in the treatment of autoimmune diseases and eye disorders, such as uveitis, iritis, and conjunctivitis. Quinoline derivatives are synthesized from 2,3-dichloroquinoline by acylation reactions with fatty acids or hydroxide solution. These derivatives show synergistic interactions with other drugs used in the treatment of inflammatory diseases such as asthma or rheumatoid arthritis. 2,3-Dichloroquinoline is also an industrial chemical that has been shown to cause environmental pollution when released into the environment. The release of this chemical is regulated by law and its use is limited to industrial preparation only.

CAS 613-18-3: 2,3-dichloroquinoline

2,3-Dichloroquinoline

Ref: 10-F091642

2,3-Dichloroquinoline

Ref: 3D-FD42295

2,3-Dichloroquinoline

Ref: 54-OR931103