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7-Hydroxyquinolinone

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CAS:70500-72-0
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7-Hydroxyquinolinone manufacturers

  • 7-Hydroxyquinolinone
  • 7-Hydroxyquinolinone pictures
  • $100.00
  • 2026-05-28
  • CAS:70500-72-0
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 10000kg
7-Hydroxyquinolinone Basic information
Product Name:7-Hydroxyquinolinone
Synonyms:2,7-DIHYDROXYQUINOLINE;7-HYDROXYQUINOLINE-(1H)-2-ONE;3,4-Dihydro-7-hydroxyquinoline-2(1H)-one;3,4-DIHYDRO-7-HYDROXY-2(1H)-QUINOLINE;7-Hydroxycarbostyril;7-HYDROXY-1H-QUINOLIN-2-ONE;7-hydroxy-2-(1h)-quinolinone;7-hydroxyquinolinone
CAS:70500-72-0
MF:C9H7NO2
MW:161.16
EINECS:812-453-9
Product Categories:Aromatics Compounds;Quinoline;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Heterocycles
Mol File:70500-72-0.mol
7-Hydroxyquinolinone Structure
7-Hydroxyquinolinone Chemical Properties
Melting point 187-192°C
Boiling point 426.8±45.0 °C(Predicted)
density 1.337±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly, Sonicated)
form Solid
pka9.32±0.20(Predicted)
color Off-White to Pale Yellow
Water Solubility Water: Insoluble
Major Applicationpharmaceutical
InChIInChI=1S/C9H7NO2/c11-7-3-1-6-2-4-9(12)10-8(6)5-7/h1-5,11H,(H,10,12)
InChIKeyDBSPUDKBNOZFMX-UHFFFAOYSA-N
SMILESN1C2=C(C=CC(O)=C2)C=CC1=O
CAS DataBase Reference70500-72-0(CAS DataBase Reference)
Safety Information
WGK Germany WGK 3
HS Code 29334900
Storage Class11 - Combustible Solids
MSDS Information
7-Hydroxyquinolinone Usage And Synthesis
Chemical PropertiesOff-White Solid
Uses7-Hydroxyquinolone is a substituted carbostyril derivative used as a pharmaceutical intermediate. It is an impurity of aripiprazole quinolinone.
DefinitionChEBI: 7-hydroxyquinolin-2(1H)-one is a monohydroxyquinoline and a quinolone.
Synthesis
N-(CINNAMOYL)-3-METHOXYANILINE

127033-74-3

7-Hydroxyquinolinone

70500-72-0

General procedure for the synthesis of 7-hydroxyquinolin-2(1H)-one from N-(3-methoxyphenyl)cinnamamide: Aluminum trichloride (3.16 g, 23.69 mmol) was added batchwise to a suspension of chlorobenzene (30 mL) of compound 3 (1 g, 3.95 mmol) in an ice bath. The reaction mixture was gradually warmed up to 120 °C and kept at reflux for 3 hours. The reaction process was monitored by thin layer chromatography (TLC). After completion of the reaction, the reaction mixture was concentrated to dryness under reduced pressure and the residue was purified by silica gel column chromatography to afford compound 4 in 54% yield.

References[1] Synthesis, 1997, # 1, p. 87 - 90
[2] Tetrahedron Letters, 1999, vol. 40, # 24, p. 4505 - 4506
[3] Journal of Medicinal Chemistry, 2015, vol. 58, # 14, p. 5561 - 5578
[4] Patent: CN108101926, 2018, A. Location in patent: Paragraph 0033; 0034; 0035
[5] Patent: WO2008/24481, 2008, A2. Location in patent: Page/Page column 32
Tag:7-Hydroxyquinolinone(70500-72-0) Related Product Information
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