4-Hydroxy-7-methoxyquinoline is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. This compound features a hydroxyl group (-OH) at the 4-position and a methoxy group (-OCH3) at the 7-position of the quinoline ring, contributing to its unique chemical properties. It is typically a yellow to brown solid and is soluble in organic solvents. The presence of the hydroxyl and methoxy groups can influence its reactivity, making it a potential candidate for various chemical reactions, including those involving hydrogen bonding and electrophilic substitution. Additionally, compounds of this class have been studied for their biological activities, including antimicrobial and antitumor properties. The CAS number 82121-05-9 uniquely identifies this substance in chemical databases, facilitating its study and application in research and industry. As with many quinoline derivatives, it may also exhibit fluorescence, which can be useful in analytical applications.

4-Hydroxy-7-methoxyquinoline

82121-05-9: 7-Methoxy-4-quinolinol, 7-Methoxyquinolin-4-Ol, 7-Methoxycinnolin-4-Ol

4-Hydroxy-7-methoxyquinoline is an anti-malarial drug that belongs to the class of trimethyl, trifluoromethyl group. It is a cyclic compound and its synthesis starts with cyclization of the methyl derivative, which forms a ring. This product is used in clinical practice as an inhibitor of malarial protozoa and has been shown to have mechanistic effects on the cytochrome bc1 complex containing red blood cells. 4-Hydroxy-7-methoxyquinoline also inhibits the growth of bacteria by binding to the enzyme methionine synthase, which is involved in the biosynthesis of methionine from homocysteine. The product also has an inhibitory effect on DNA synthesis and protein synthesis.

CAS 82121-05-9: 4-Hydroxy-7-methoxyquinoline

4-Hydroxy-7-methoxyquinoline

Ref: 3D-FH42402

4-Hydroxy-7-methoxyquinoline

Ref: IN-DA0051ID

7-Methoxy-4-quinolinol

Ref: 3B-M1966

4-Hydroxy-7-methoxyquinoline

Ref: 54-OR8294