6-BROMO-2-HYDROXYQUINOLINE-4-CARBOXYLIC ACID
6-BROMO-2-HYDROXYQUINOLINE-4-CARBOXYLIC ACID Basic information
- Product Name:
- 6-BROMO-2-HYDROXYQUINOLINE-4-CARBOXYLIC ACID
- Synonyms:
-
- 6-bromo-2-keto-1H-quinoline-4-carboxylic acid
- 6-bromo-2-oxo-1H-quinoline-4-carboxylic acid
- 4-Quinolinecarboxylic acid, 6-bromo-1,2-dihydro-2-oxo-
- 6-Bromo-2-oxo-1,2-dihydroquinoline-5-carboxylic acid
- CAS:
- 5463-29-6
- MF:
- C10H6BrNO3
- MW:
- 268.06
- Mol File:
- 5463-29-6.mol
6-BROMO-2-HYDROXYQUINOLINE-4-CARBOXYLIC ACID Chemical Properties
- Boiling point:
- 446.7±45.0 °C(Predicted)
- Density
- 1.804±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 2.54±0.20(Predicted)
- Appearance
- Off-white to light yellow Solid
6-BROMO-2-HYDROXYQUINOLINE-4-CARBOXYLIC ACID Usage And Synthesis
Synthesis
541-50-4
87-48-9
5463-29-6
6-Bromo-2-hydroxy-4-carboxylic acid quinoline was synthesized using the method described in Scheme 6. The procedure was as follows: 5-bromoindoline-2,3-dione (0.250 g) was dissolved in tetrahydrofuran (THF, 3 ml) in a round-bottomed flask, followed by the addition of malonic acid (2 equiv). The unit was connected to a reflux condenser and heated to reflux by conventional heating and the reaction was continued overnight. After 12 hours of reaction, a solid precipitate was observed to be generated. Subsequently, the suspension was concentrated under reduced pressure to remove the solvent, and the suspension was refluxed for 4 hours after addition of an appropriate amount of water. Finally, the solid product was collected by filtration to afford 6-bromo-2-hydroxyquinoline-4-carboxylic acid (0.150 g) in solid form.
References
[1] Patent: US2014/221387, 2014, A1. Location in patent: Paragraph 0383; 0384; 0385
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6-BROMO-2-HYDROXYQUINOLINE-4-CARBOXYLIC ACID(5463-29-6)Related Product Information
- 2-Hydroxy-4-pyridinecarboxaldehyde
- 6-Bromo-4-methylquinoline
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- CHEMBRDG-BB 6599056
- 2-Quinolinol
- 6-BROMO-2-HYDROXYQUINOLINE-4-CARBOXYLIC ACID
- 6-Bromoquinoline
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