ChemicalBook--->CAS DataBase List--->59394-30-8

59394-30-8

59394-30-8 Structure

59394-30-8 Structure
IdentificationBack Directory
[Name]

6-CHLOROQUINOLINE-2-CARBOXYLIC ACID
[CAS]

59394-30-8
[Synonyms]

AKOS A0602-0951
6-Chloro-2-quinolinecarboxylic acid
6-CHLOROQUINOLINE-2-CARBOXYLIC ACID
2-Quinolinecarboxylic acid, 6-chloro-
[Molecular Formula]

C10H6ClNO2
[MDL Number]

MFCD09834123
[MOL File]

59394-30-8.mol
[Molecular Weight]

207.61
Chemical PropertiesBack Directory
[Melting point ]

228 °C
[Boiling point ]

382.1±27.0 °C(Predicted)
[density ]

1.469±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

4.45±0.43(Predicted)
[Appearance]

White to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

6-CHLOROQUINOLINE-2-CARBOXYLIC ACID(59394-30-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-CHLOROQUINOLINE-2-CARBALDEHYDE

59394-26-2

6-CHLOROQUINOLINE-2-CARBOXYLIC ACID

59394-30-8

General procedure for the synthesis of 6-chloro-2-quinoline carboxylic acid from 6-chloro-2-quinoline carboxaldehyde: A solution of sodium chlorite (2.4 g) and sodium dihydrogen phosphate (2.4 g) in water (24 ml) was added slowly and dropwise over a period of 5 min to a solution of 6-chloroquinoline-2-carboxaldehyde (536 mg; 2.8 mmol) dissolved in a tert-butanol (56 ml) and 2-methyl-2-butene (14 ml) mixed solution. The reaction mixture was stirred at room temperature for 4 hours. After completion of the reaction, the organic solvent was removed by distillation under reduced pressure. Water (30 ml) was added to the residue and a white precipitate was precipitated. The precipitate was collected by filtration, washed with water and dried under vacuum in the presence of phosphorus pentoxide to afford 6-chloroquinoline-2-carboxylic acid in white powder form (505 mg; yield = 87%). Mass spectrometry/liquid chromatography analysis: m/z=208.01 (M+H), retention time=8.55 min (condition 1). NMR hydrogen spectrum (DMSO-d6,400MHz) δ: 8.41-8.39 (m, 1H, aromatic H); 8.20-8.11 (m, 3H, aromatic H); 7.82-7.79 (m, 1H, aromatic H).

[References]

[1] Patent: US2005/154039, 2005, A1. Location in patent: Page/Page column 11
[2] Tetrahedron, 2013, vol. 69, # 38, p. 8209 - 8215
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59394-26-2