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CAS 898752-37-9

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Ethyl 3,5-difluoro-δ-oxobenzenepentanoate

Description:
Ethyl 3,5-difluoro-δ-oxobenzenepentanoate is a chemical compound characterized by its unique structure, which includes an ethyl ester functional group and a substituted aromatic ring. The presence of two fluorine atoms at the 3 and 5 positions of the benzene ring contributes to its reactivity and potential applications in various chemical reactions. The δ-oxobenzenepentanoate structure indicates that it contains a ketone functional group adjacent to a pentanoate chain, which can influence its physical properties, such as solubility and boiling point. This compound may exhibit interesting biological activities due to the fluorine substituents, which can enhance lipophilicity and metabolic stability. Additionally, the presence of the ethyl ester group suggests potential for hydrolysis reactions, making it relevant in synthetic organic chemistry. Overall, Ethyl 3,5-difluoro-δ-oxobenzenepentanoate is a compound of interest for research in medicinal chemistry and materials science, although specific applications would depend on further studies and evaluations of its properties.
Formula:C13H14F2O3
InChI:InChI=1S/C13H14F2O3/c1-2-18-13(17)5-3-4-12(16)9-6-10(14)8-11(15)7-9/h6-8H,2-5H2,1H3
InChI key:InChIKey=YHOZKHKNHDDFEL-UHFFFAOYSA-N
SMILES:C(CCCC(OCC)=O)(=O)C1=CC(F)=CC(F)=C1
Synonyms:
  • Benzenepentanoic acid, 3,5-difluoro-δ-oxo-, ethyl ester
  • Ethyl 5-(3,5-difluorophenyl)-5-oxovalerate
  • Ethyl 3,5-difluoro-δ-oxobenzenepentanoate
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