ChemicalBook--->CAS DataBase List--->5467-57-2

5467-57-2

5467-57-2 Structure

5467-57-2 Structure
IdentificationMore
[Name]

2-CHLOROQUINOLINE-4-CARBOXYLIC ACID
[CAS]

5467-57-2
[Synonyms]

2-CHLORO-4-CARBOXY QUINOLINE
2-CHLOROQUINOLINE-4-CARBOXYLIC ACID
A-CHLORO CINCHONINIC ACID
AKOS BB-6908
2-chloroquinazoline-4-carboxylic acid ethyl ester
[Molecular Formula]

C10H6ClNO2
[MDL Number]

MFCD00023940
[Molecular Weight]

207.61
[MOL File]

5467-57-2.mol
Chemical PropertiesBack Directory
[Melting point ]

244 °C
[Boiling point ]

368.7±22.0 °C(Predicted)
[density ]

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

Keep in dark place,Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

2.17±0.10(Predicted)
[color ]

White to Orange to Green
[InChI]

InChI=1S/C10H6ClNO2/c11-9-5-7(10(13)14)6-3-1-2-4-8(6)12-9/h1-5H,(H,13,14)
[InChIKey]

ICNCOMYUODLTAI-UHFFFAOYSA-N
[SMILES]

N1C2C(=CC=CC=2)C(C(O)=O)=CC=1Cl
[CAS DataBase Reference]

5467-57-2(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[HazardClass ]

IRRITANT
[HS Code ]

2933491090
Hazard InformationBack Directory
[Uses]

2-Chloroquinoline-4-carboxylic Acid is an intermediate used to prepare dimethyl(naphthalenecarbonyl)aminobenzoic acids as potent and selective EP4 antagonists.
[Synthesis]

2-Hydroxy-4-quinolincarboxylic acid

15733-89-8

2-CHLOROQUINOLINE-4-CARBOXYLIC ACID

5467-57-2

The general procedure for the synthesis of 2-chloroquinoline-4-carboxylic acid from 2-quinolone-4-carboxylic acid was as follows: 2-hydroxyquinoline-4-carboxylic acid (2.57 g, 13.6 mmol) was mixed with phosphorus oxytriphosphate (POCl3, 25 mL) and heated and refluxed for 24 hours. Upon completion of the reaction, the reaction mixture was quenched by slowly pouring it into crushed ice (300 g). The precipitated solid was separated by filtration, washed thoroughly with deionized water and dried under high vacuum to give 2.47 g of white solid product in 87% yield. The product was characterized by 1H NMR (CDCl3, 300 MHz) and LCMS: 1H NMR δ 8.67 (d, 1H, J = 8.4 Hz), 7.91 (d, 1H, J = 8.1 Hz), 7.83 (s, 1H), 7.67 (t, 1H, J = 7.2 Hz), 7.54 (t, 1H, J = 7.2 Hz); LCMS (m/ z): 208 ([M+H]+).

[References]

[1] Patent: WO2005/30774, 2005, A1. Location in patent: Page/Page column 23
[2] Journal of the American Chemical Society, 1946, vol. 68, p. 1837,1838
[3] Proceedings of the Royal Society of London, Series B: Biological Sciences, 1938, vol. 125, p. 60,69
Spectrum DetailBack Directory
[Spectrum Detail]

2-CHLOROQUINOLINE-4-CARBOXYLIC ACID(5467-57-2)1HNMR
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

2-Chloroquinoline-4-carboxylic Acid,>97.0%(LC)(T)(5467-57-2)
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