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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Quinoline compounds >  Ethyl 6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate

Ethyl 6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate

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Ethyl 6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate Basic information

Product Name:
Ethyl 6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate
Synonyms:
  • ETHYL 6,7,8-TRIFLUORO-1,4-DIHYDRO-4-OXO-3-QUINOLINECARBOXYLATE
  • ETHYL 6,7,8-TRIFLUORO-4-OXOHYDROQUINOLINE-3-CARBOXYLATE
  • 1,4-dihydro-4-oxo-6,7,8-trifluoro-3-quinolinecarboxylicaciethylester
  • dm-7
  • ethyl1,4-dihydro-4-oxo-6,7,8-trifluoro-3-quinolinecarboxylate
  • CycliccompoundofLomefloxacin
  • 6,7,8-Trifluoro-1,4-Dihydro-4-Oxo-3-Quinolinecarboxylic Acid Ethyl Ester
  • 3-ethoxycarbonyl-6,7,8-trifluoro-1,4-hydro-4-oxoquinoline
CAS:
79660-46-1
MF:
C12H8F3NO3
MW:
271.19
Product Categories:
  • Building Blocks
  • C11 to C30
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Quinolines
Mol File:
79660-46-1.mol
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Ethyl 6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate Chemical Properties

Melting point:
275 °C (dec.) (lit.)
Boiling point:
344.3±42.0 °C(Predicted)
Density 
1.451
storage temp. 
Sealed in dry,Room Temperature
pka
-0.92±0.70(Predicted)
Appearance
Off-white to light brown Solid
CAS DataBase Reference
79660-46-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
2
RTECS 
VB2009830
HazardClass 
IRRITANT
HS Code 
29334910

MSDS

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Ethyl 6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate Usage And Synthesis

Chemical Properties

beige to beige-brown powder

General Description

Ethyl 6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate is also referred to as 3-ethoxycarbonyl-6,7,8-trifluoro-1,4-hydro-4-oxoquinoline.

Synthesis

100501-60-8

79660-46-1

General procedure for the synthesis of ethyl 6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate from diethyl 2-[[(2,3,4-trifluorophenyl)amino]methylene]malonate: Compound 2 (5.30 g, 16.70 mmol) was dissolved in diphenyl ether (35 mL), and the reaction was carried out at reflux for 8 hr at 250 °C. After completion of the reaction, the reaction mixture was cooled and the precipitate precipitated was collected by filtration. The precipitate was washed with hexane and subsequently recrystallized with ethanol to give the target product 3 as a white solid.

References

[1] Synthetic Communications, 2009, vol. 39, # 24, p. 4375 - 4383
[2] Tetrahedron, 2007, vol. 63, # 9, p. 2093 - 2097
[3] European Journal of Medicinal Chemistry, 2011, vol. 46, # 4, p. 1232 - 1244
[4] Tetrahedron, 1992, vol. 48, # 29, p. 6135 - 6150
[5] Magnetic Resonance in Chemistry, 1996, vol. 34, # 11, p. 972 - 978

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