CAS 2598-30-3
:8-hydroxyquinoline-5-carbaldehyde
Description:
8-Hydroxyquinoline-5-carbaldehyde is an organic compound characterized by its quinoline structure, which features a hydroxyl group and an aldehyde functional group. This compound typically appears as a yellow to brown solid and is known for its ability to chelate metal ions, making it useful in various applications, including analytical chemistry and materials science. The presence of the hydroxyl group enhances its solubility in polar solvents, while the aldehyde group can participate in further chemical reactions, such as condensation and oxidation. 8-Hydroxyquinoline-5-carbaldehyde is also recognized for its potential biological activities, including antimicrobial and anticancer properties, which have been the subject of research in medicinal chemistry. Its unique structural features contribute to its reactivity and versatility in synthetic applications, making it a valuable compound in both academic and industrial settings. Safety precautions should be observed when handling this substance, as it may pose health risks if ingested or inhaled.
Formula:C10H7NO2
InChI:InChI=1/C10H7NO2/c12-6-7-3-4-9(13)10-8(7)2-1-5-11-10/h1-6,13H
SMILES:c1cc2c(ccc(c2nc1)O)C=O
Synonyms:- 5-Quinolinecarboxaldehyde, 8-Hydroxy-
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Found 5 products.
5-Quinolinecarboxaldehyde, 8-hydroxy-
CAS:Formula:C10H7NO2Purity:95%Color and Shape:SolidMolecular weight:173.16818-Hydroxyquinoline-5-carbaldehyde
CAS:Formula:C10H7NO2Purity:98%Color and Shape:SolidMolecular weight:173.1718-Hydroxyquinoline-5-carbaldehyde
CAS:Controlled Product<p>Applications 8-Hydroxyquinoline-5-carbaldehyde is used in preparation of Polycyclic compounds.<br>References Zeng, Y., et al.: PCT Int. Appl., (2018);<br></p>Formula:C10H7NO2Color and Shape:NeatMolecular weight:173.168-hydroxy-quinoline-5-carbaldehyde
CAS:<p>8-hydroxy-quinoline-5-carbaldehyde (8HQ) is a quinoline derivative that can bind to metal ions. It has antiviral properties and can be used to treat HIV, Hepatitis B and C, as well as influenza. 8HQ is synthesized by the reaction of sodium salts and 5-hydroxy-2,4-quinolinediol in aqueous solution at pH 11. The reactants are coordinated with the metal ion before the addition of trifluoroacetic acid. Computational methods have been employed to study this process.</p>Formula:C10H7NO2Purity:Min. 95%Molecular weight:173.17 g/mol




