2-Chloro-6-nitroquinoline is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a chlorine atom at the second position and a nitro group at the sixth position of the quinoline ring significantly influences its chemical properties and reactivity. This compound typically appears as a yellow to orange crystalline solid and is known for its potential applications in medicinal chemistry, particularly in the development of antimicrobial and antitumor agents. It exhibits moderate solubility in organic solvents, while its solubility in water is limited. The nitro group contributes to its electrophilic character, making it a potential candidate for further chemical modifications. Additionally, 2-chloro-6-nitroquinoline may exhibit biological activity, which has been the subject of various studies aimed at understanding its mechanism of action and therapeutic potential. As with many chemical substances, appropriate safety measures should be taken when handling this compound due to its potential toxicity and environmental impact.

2-Chloro-6-nitroquinoline

29969-57-1: Quinoline, 2-Chloro-6-Nitro-, 2-Chloro-6-nitroquinoline

2-Chloro-6-nitroquinoline (CNDQ) is a synthetic compound that is used as an analog of serotonin. This compound has been shown to be a potent and selective serotonin reuptake inhibitor in vivo, with affinities for the serotonin transporter that are more than 100 times greater than other monoamine transporters. CNDQ has also been observed to inhibit the uptake of dopamine and norepinephrine, which may account for its antidepressant activity. The alkyl groups on this molecule enhance its binding affinity for amine receptors.

CAS 29969-57-1: 2-Chloro-6-nitroquinoline

2-Chloro-6-nitroquinoline

Ref: 54-OR927639

2-Chloro-6-nitroquinoline

Ref: 3D-FC42127

2-CHLORO-6-NITROQUINOLINE

Ref: IN-DA00C4E2

2-Chloro-6-nitroquinoline

Ref: 10-F210689