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CAS 342636-36-6

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Ethyl 4-fluoro-δ-oxobenzenepentanoate

Description:
Ethyl 4-fluoro-δ-oxobenzenepentanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of a carboxylic acid and an alcohol. This compound features a fluoro substituent on the aromatic ring, which can influence its reactivity and physical properties, such as polarity and solubility. The presence of the δ-oxobenzene moiety indicates that it contains a ketone functional group adjacent to the aromatic system, contributing to its potential reactivity in various chemical reactions, including nucleophilic additions and condensation reactions. Ethyl 4-fluoro-δ-oxobenzenepentanoate may exhibit interesting biological activities, making it a candidate for pharmaceutical applications. Its molecular structure suggests that it could be soluble in organic solvents, while its stability and reactivity would depend on the specific conditions of use. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards. Overall, this compound represents a unique combination of functional groups that may be of interest in synthetic organic chemistry and medicinal chemistry research.
Formula:C13H15FO3
InChI:InChI=1/C13H15FO3/c1-2-17-13(16)5-3-4-12(15)10-6-8-11(14)9-7-10/h6-9H,2-5H2,1H3
InChI key:InChIKey=TWLQYFQKWODQQD-UHFFFAOYSA-N
SMILES:C(CCCC(OCC)=O)(=O)C1=CC=C(F)C=C1
Synonyms:
  • Ethyl 5-oxo-5-(4-fluorophenyl)pentanoate
  • Ethyl 4-fluoro-δ-oxobenzenepentanoate
  • Benzenepentanoic acid, 4-fluoro-δ-oxo-, ethyl ester
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