ChemicalBook--->CAS DataBase List--->13720-94-0

13720-94-0

13720-94-0 Structure

13720-94-0 Structure
IdentificationMore
[Name]

ETHYL 4-CHLORO-3-QUINOLINECARBOXYLATE
[CAS]

13720-94-0
[Synonyms]

4-CHLORO-QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER
AURORA 18125
ETHYL 4-CHLORO-3-QUINOLINECARBOXYLATE
ETHYL 4-CHLOROQUINOLINE-3-CARBOXYLATE
[Molecular Formula]

C12H10ClNO2
[MDL Number]

MFCD00173407
[Molecular Weight]

235.67
[MOL File]

13720-94-0.mol
Chemical PropertiesBack Directory
[Melting point ]

46-48°C
[Boiling point ]

128-129 °C(Press: 0.2 Torr)
[density ]

1.286
[storage temp. ]

Storage temp. -20°C
[form ]

powder to crystal
[pka]

1.78±0.24(Predicted)
[color ]

White to Orange to Green
[InChIKey]

DWXQUAHMZWZXHP-UHFFFAOYSA-N
[CAS DataBase Reference]

13720-94-0(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 .
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2933499090
Hazard InformationBack Directory
[Uses]

Ethyl 4-chloroquinoline-3-carboxylate is used as organic chemical synthesis intermediate.
[Synthesis]

4-HYDROXYQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER

26892-90-0

ETHYL 4-CHLORO-3-QUINOLINECARBOXYLATE

13720-94-0

Synthesis of ethyl 4-chloroquinoline-3-carboxylate (A2): ethyl 4-hydroxyquinoline-3-carboxylate (A1) (1.5 g, 7 mmol) solid was placed in a reaction vial and phosphorus oxychloride (POCl3) (2.2 g, 1.3 mL, 14 mmol) was added. The reaction mixture was heated at 110 °C for 20 min. Upon completion of the reaction, the mixture was slowly poured into a pre-cooled mixture of aqueous ammonia solution (28-30%) and ice and stirred until a granular solid was formed. The reaction mixture was extracted with ether (3 x 40 mL), the organic layers were combined, dried with anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure to give an oily product. After standing, the product crystallized (1.44 g, 6 mmol, 87% yield) and could be used for subsequent reactions without further purification.

[References]

[1] Journal of Medicinal Chemistry, 2006, vol. 49, # 21, p. 6351 - 6363
[2] Patent: WO2005/123686, 2005, A1. Location in patent: Page/Page column 75-76
[3] European Journal of Medicinal Chemistry, 2015, vol. 103, p. 1 - 16
[4] Patent: CN108623589, 2018, A. Location in patent: Paragraph 0142; 0149
[5] Patent: CN108623581, 2018, A. Location in patent: Page/Page column 7
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL 4-CHLORO-3-QUINOLINECARBOXYLATE(13720-94-0)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

Ethyl 4-chloroquinoline-3-carboxylate(13720-94-0)
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