6-Iodoquinolin-2-ol is a chemical compound characterized by its quinoline structure, which features a hydroxyl group (-OH) and an iodine atom at the 6-position of the quinoline ring. This compound typically exhibits properties such as being a pale yellow to brown solid, with moderate solubility in organic solvents and limited solubility in water due to its aromatic nature. The presence of the hydroxyl group contributes to its potential as a ligand in coordination chemistry, while the iodine substituent can enhance its reactivity and influence its biological activity. 6-Iodoquinolin-2-ol may also exhibit antimicrobial or antifungal properties, making it of interest in medicinal chemistry. Its molecular structure allows for various chemical modifications, which can lead to derivatives with altered pharmacological profiles. As with many halogenated compounds, safety precautions should be taken when handling due to potential toxicity and environmental impact.

6-iodoquinolin-2-ol

6-Iodo-1H-Quinolin-2-One

6-Iodoquinolin-2-ol is a heterocyclic organic compound that is synthesized from anilines, sulfuric acid, and electron donors. This compound has been shown to react with amides and quinolines to form heterocycles. 6-Iodoquinolin-2-ol can be used in the synthesis of other heterocycles that have electron donating groups or functional groups on them. The sequence of reactions for this process is scalable, which means it can be scaled up or down to suit the needs of the experimenter.

CAS 99455-01-3: 6-iodoquinolin-2-ol

6-Iodo-1H-Quinolin-2-One

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6-Iodoquinolin-2-ol

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6-Iodoquinolin-2(1H)-one

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6-Iodoquinolin-2-ol

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