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4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER

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4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER Basic information

Product Name:
4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER
Synonyms:
  • ETHYL 4-HYDROXYQUINOLINE-3-CARBOXYLATE
  • 4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER
  • 4-Hydroxyquinoline-3-carboxylic acid ethyl ester 98%
  • 4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER, 95+%
  • 4-keto-1H-quinoline-3-carboxylic acid ethyl ester
  • ethyl 4-oxo-1H-quinoline-3-carboxylate
  • 3-Quinolinecarboxylic acid, 4-hydroxy-, ethyl ester
  • 3-Ethoxycarbonyl-4-quinolinol
CAS:
26892-90-0
MF:
C12H11NO3
MW:
217.22
EINECS:
803-448-2
Product Categories:
  • Acids and Derivatives
  • Heterocycles
Mol File:
26892-90-0.mol
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4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER Chemical Properties

Melting point:
271°C(lit.)
Boiling point:
334.9±22.0 °C(Predicted)
Density 
1.280±0.06 g/cm3(Predicted)
storage temp. 
Store at room temperature
pka
2.62±0.50(Predicted)
form 
powder to crystal
color 
White to Light yellow to Light orange
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26
WGK Germany 
3
HS Code 
2933499090
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4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER Usage And Synthesis

Synthesis

54535-22-7

26892-90-0

General procedure for the synthesis of ethyl 4-hydroxyquinoline-3-carboxylate from diethyl 2-phenylaminomethylidene-malonate: In a 1L three-necked flask fitted with a mechanical stirrer, diethyl 2-phenylaminomethylidene-malonate (26.3 g, 0.100 mol), polyphosphoric acid (270 g), and phosphorochloride (750 g) were added. The reaction mixture was heated to 70 °C and stirred at this temperature for 4 hours. After completion of the reaction, the mixture was cooled to room temperature and then filtered. The filtered residue was treated with aqueous sodium carbonate (Na2CO3), filtered again, washed with water and finally dried. Ethyl 4-hydroxyquinoline-3-carboxylate was obtained as a light brown solid (15.2 g, 70% yield).

References

[1] Patent: US4079058, 1978, A
[2] Patent: US2008/90864, 2008, A1. Location in patent: Page/Page column 7
[3] Patent: WO2007/79139, 2007, A2. Location in patent: Page/Page column 46
[4] European Journal of Medicinal Chemistry, 2015, vol. 103, p. 1 - 16
[5] Molecular Crystals and Liquid Crystals Science and Technology Section A: Molecular Crystals and Liquid Crystals, 2000, vol. 344, p. 163 - 168

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