Quinoline, 6,8-dimethoxy- is an organic compound characterized by its quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of two methoxy groups (-OCH3) at the 6 and 8 positions of the quinoline structure significantly influences its chemical properties and reactivity. This compound is typically a pale yellow to brown liquid or solid, depending on its purity and specific conditions. It is known for its aromatic nature, which contributes to its stability and potential applications in various fields, including pharmaceuticals and agrochemicals. Quinoline derivatives often exhibit biological activity, making them of interest in medicinal chemistry. The methoxy substituents can enhance solubility in organic solvents and may also affect the compound's interaction with biological targets. As with many quinoline derivatives, it is essential to handle this compound with care, considering potential toxicity and environmental impact. Overall, 6,8-dimethoxyquinoline represents a unique structure within the quinoline family, with promising applications in research and industry.

Quinoline, 6,8-dimethoxy-

111454-91-2: Quinoline, 6,8-dimethoxy- is an organic compound characterized by its quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of two methoxy groups (-OCH3) at the 6 and 8 positions of the quinoline structure significantly influences its chemical properties and reactivity. This compound is typically a pale yellow to brown liquid or solid, depending on its purity and specific conditions. It is known for its aromatic nature, which contributes to its stability and potential applications in various fields, including pharmaceuticals and agrochemicals. Quinoline derivatives often exhibit biological activity, making them of interest in medicinal chemistry. The methoxy substituents can enhance solubility in organic solvents and may also affect the compound's interaction with biological targets. As with many quinoline derivatives, it is essential to handle this compound with care, considering potential toxicity and environmental impact. Overall, 6,8-dimethoxyquinoline represents a unique structure within the quinoline family, with promising applications in research and industry.

6,8-Dimethoxyquinoline

<p>6,8-Dimethoxyquinoline is a quinoline derivative that has been used to synthesize a number of other drugs. It has shown activity against cancer cells in vitro and in vivo and has been shown to have an anticholinergic effect on the central nervous system. 6,8-Dimethoxyquinoline also inhibits bacterial growth and is active against Gram-positive bacteria such as Enterococcus faecalis, Staphylococcus aureus, Streptococcus pyogenes, and Bacillus subtilis. This compound binds to the enzyme carbonic anhydrase II with high affinity. The binding of 6,8-dimethoxyquinoline with carbonic anhydrase II prevents the conversion of CO2 into carbonic acid, which may lead to cell death by inhibiting respiration.</p>

CAS 111454-91-2

Quinoline, 6,8-dimethoxy-

6,8-Dimethoxyquinoline

Ref: IN-DA00HC59

6,8-Dimethoxyquinoline

Ref: 3D-LEA45491