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CAS 426842-72-0

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3-Chloro-6-methoxy-4-quinolinol

Description:
3-Chloro-6-methoxy-4-quinolinol is a chemical compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a chlorine atom at the 3-position and a methoxy group at the 6-position contributes to its unique chemical properties. This compound typically exhibits a pale yellow to brownish appearance and is soluble in organic solvents, while its solubility in water may be limited. It is often studied for its potential biological activities, including antimicrobial and antitumor properties, due to the presence of the quinolinol moiety, which is known for its ability to chelate metal ions and interact with biological targets. The compound's reactivity can be influenced by the electron-withdrawing nature of the chlorine atom and the electron-donating characteristics of the methoxy group, which can affect its interactions in various chemical environments. As with many quinoline derivatives, it may also exhibit fluorescence, making it useful in certain analytical applications.
Formula:C10H8ClNO2
InChI:InChI=1/C10H8ClNO2/c1-14-6-2-3-9-7(4-6)10(13)8(11)5-12-9/h2-5H,1H3,(H,12,13)
InChI key:InChIKey=RDNOZYLIMZPTDV-UHFFFAOYSA-N
SMILES:OC=1C2=C(C=CC(OC)=C2)N=CC1Cl
Synonyms:
  • 3-Chloro-4-hydroxy-6-methoxyquinoline
  • 3-Chloro-6-methoxy-1H-quinolin-4-one
  • 3-Chloro-6-methoxy-4-quinolinol
  • 4-Quinolinol, 3-Chloro-6-Methoxy-
  • 3-Chloro-6-methoxyquinolin-4-ol
  • 3-Chloro-6-methoxyquinoline-4-ol
  • 3-CHLORO-6-METHOXYQUINOLIN-4(1H)-ONE
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