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Ethyl 3-(4-fluorophenyl)-3-oxopropanoate

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Ethyl 3-(4-fluorophenyl)-3-oxopropanoate Basic information

Product Name:
Ethyl 3-(4-fluorophenyl)-3-oxopropanoate
Synonyms:
  • (4-FLUOROBENZOYL)ACETIC ACID ETHYL ESTER
  • 3-(4'-Fluorophenyl)-3-oxopropanoate
  • ETHYL 3-(4'-FLUOROPHENYL)-3-OXOPROPNOATE
  • ETHYL 4-FLUOROBENZOYLACETATE
  • ETHYL (P-FLUOROBENZOYL)ACETATE
  • 3-(4-FLUORO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER
  • 3-Oxo-3-(4-fluorophenyl)propanoic acid ethyl ester
  • p-Fluorobenzoylacetic acid ethyl ester
CAS:
1999-00-4
MF:
C11H11FO3
MW:
210.2
Product Categories:
  • Benzene series
  • Benzoic acid
  • Acids & Esters
  • Fluorine Compounds
Mol File:
1999-00-4.mol
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Ethyl 3-(4-fluorophenyl)-3-oxopropanoate Chemical Properties

Melting point:
117-120℃
Boiling point:
117-120 °C(lit.)
Density 
1.174 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.5040(lit.)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
clear liquid
pka
9.82±0.25(Predicted)
Specific Gravity
1.19
color 
Colorless to Almost colorless
InChIKey
SJUXLKYJKQBZLM-UHFFFAOYSA-N
CAS DataBase Reference
1999-00-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Safety Statements 
24/25
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29183000

MSDS

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Ethyl 3-(4-fluorophenyl)-3-oxopropanoate Usage And Synthesis

Chemical Properties

Colorless liquid

Uses

Reactant used as a precursor in:

  • Condensation reactions with diamines via C-C bond cleavage for synthesis of benzimidazoles and perimidines for possible use as antimalarial treatments
  • Base-promoted domino Michael addition / cyclization / elimination reactions for synthesis of hydroxybenzophenones
  • Oxidative cross-coupling with indoles via dioxygen activation
  • Cyclization of keto esters for synthesis of pyrones
  • Lewis base catalyzed hydrosilylation for synthesis of α-acetoxy β-amino acid derivatives
  • Conia-ene reactions for synthesis of methylenecyclopentane derivatives

General Description

Ethyl (4-fluorobenzoyl)acetate on condensation with benzofurazan oxide yields 2-(carboethoxy)-3-(4′-fluoro)phenylquinoxaline1,4-dioxide.

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