2,6-Dichloroquinoline is a heterocyclic aromatic compound characterized by a quinoline structure with two chlorine substituents at the 2 and 6 positions. It is a pale yellow to brown solid at room temperature and is known for its relatively low solubility in water, while being more soluble in organic solvents such as ethanol and acetone. The presence of chlorine atoms enhances its reactivity, making it useful in various chemical syntheses and applications, including as an intermediate in the production of pharmaceuticals and agrochemicals. 2,6-Dichloroquinoline exhibits biological activity, which has been explored in medicinal chemistry, particularly for its potential antimicrobial and antimalarial properties. Its molecular formula is C9H6Cl2N, and it has a distinct aromatic character due to the conjugated double bond system in the quinoline ring. Safety precautions should be observed when handling this compound, as it may pose health risks, including potential toxicity and environmental hazards.

2,6-Dichloroquinoline

1810-72-6: Quinoline, 2,6-dichloro-, 2,6-Dichloroquinoline

2,6-Dichloroquinoline is a chlorinated aromatic compound that reacts with amines to form quinoline derivatives. It can be synthesized by the reaction of 2,6-dichlorophenol with chloroacetyl chloride. 2,6-Dichloroquinoline is an organic solvent that has been used in the synthesis of pharmaceuticals and as a solvent for certain types of paints. The pharmacokinetic properties of 2,6-dichloroquinoline have been studied in vivo using rats. It is believed to be metabolized through the liver and excreted in urine via the kidneys.

CAS 1810-72-6: 2,6-Dichloroquinoline

2,6-Dichloroquinoline

Ref: 3B-D5429

2,6-Dichloroquinoline

Ref: 3D-FD149582

2,6-Dichloroquinoline

Ref: 10-F223672

2,6-Dichloroquinoline

Ref: 54-OR307515

Quinoline, 2,6-dichloro-

Ref: IN-DA0022JJ