| Identification | Back Directory | [Name]
4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER | [CAS]
26892-90-0 | [Synonyms]
3-Ethoxycarbonyl-4-quinolinol
ethyl 4-oxo-1H-quinoline-3-carboxylate
ETHYL 4-HYDROXYQUINOLINE-3-CARBOXYLATE
Ethyl4-Hydroxyquinoline-3-carboxylate>
4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER
4-keto-1H-quinoline-3-carboxylic acid ethyl ester
3-Quinolinecarboxylic acid, 4-hydroxy-, ethyl ester
4-Hydroxyquinoline-3-carboxylic acid ethyl ester 98%
4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER, 95+%
4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER ISO 9001：2015 REACH | [EINECS(EC#)]
803-448-2 | [Molecular Formula]
C12H11NO3 | [MDL Number]
MFCD00173406 | [MOL File]
26892-90-0.mol | [Molecular Weight]
217.22 |
| Chemical Properties | Back Directory | [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 | [form ]
powder to crystal | [pka]
2.62±0.50(Predicted) | [color ]
White to Light yellow to Light orange | [InChI]
1S/C12H11NO3/c1-2-16-12(15)9-7-13-10-6-4-3-5-8(10)11(9)14/h3-7H,2H2,1H3,(H,13,14) | [InChIKey]
YBEOYBKKSWUSBR-UHFFFAOYSA-N | [SMILES]
CCOC(=O)c1cnc2ccccc2c1O |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H319 | [Precautionary statements ]
P305+P351+P338 | [Hazard Codes ]
Xi | [Risk Statements ]
36 | [Safety Statements ]
26 | [WGK Germany ]
3 | [HS Code ]
2933499090 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2 |
| Hazard Information | Back Directory | [Synthesis]
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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