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CAS 5220-02-0

:

3-Amino-6-chloro-1-methyl-4-phenyl-2(1H)-quinolinone

Description:
3-Amino-6-chloro-1-methyl-4-phenyl-2(1H)-quinolinone, with the CAS number 5220-02-0, is a synthetic organic compound belonging to the quinolinone class. This compound features a quinoline core structure, which is characterized by a fused bicyclic system containing a benzene ring and a pyridine ring. The presence of an amino group at the 3-position and a chloro substituent at the 6-position contributes to its reactivity and potential biological activity. The methyl group at the 1-position and the phenyl group at the 4-position enhance its lipophilicity, which may influence its pharmacokinetic properties. This compound is of interest in medicinal chemistry due to its potential applications in drug development, particularly in the fields of anti-inflammatory and antimicrobial agents. Its solubility, stability, and interaction with biological targets can vary based on the specific conditions and solvents used. As with many quinolinone derivatives, it may exhibit a range of biological activities, making it a subject of research in various therapeutic areas.
Formula:C16H13ClN2O
InChI:InChI=1S/C16H13ClN2O/c1-19-13-8-7-11(17)9-12(13)14(15(18)16(19)20)10-5-3-2-4-6-10/h2-9H,18H2,1H3
InChI key:InChIKey=GHUMMQSCMAWOQZ-UHFFFAOYSA-N
SMILES:NC1=C(C=2C(N(C)C1=O)=CC=C(Cl)C2)C3=CC=CC=C3
Synonyms:
  • 2(1H)-Quinolone, 3-amino-6-chloro-1-methyl-4-phenyl-
  • 2(1H)-quinolinone, 3-amino-6-chloro-1-methyl-4-phenyl-
  • 3-Amino-1,2-dihydro-6-chloro-1-methyl-4-phenylquinolin-2(1H)-one
  • 3-Amino-6-chloro-1-methyl-4-phenyl-2(1H)-quinolinone
  • 3-Amino-6-chloro-1-methyl-4-phenylcarbostyril
  • 3-Amino-6-chloro-1-methyl-4-phenylquinolin-2-one
  • Carbostyril, 3-amino-6-chloro-1-methyl-4-phenyl-
  • 3-Amino-6-chloro-1-methyl-4-phenylquinolin-2(1H)-one
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