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CAS 362669-42-9

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Ethyl η-oxo-4-(trifluoromethyl)benzeneoctanoate

Description:
Ethyl η-oxo-4-(trifluoromethyl)benzeneoctanoate, identified by its CAS number 362669-42-9, is an organic compound characterized by its complex structure, which includes an ethyl ester functional group, a ketone (η-oxo) moiety, and a trifluoromethyl group attached to a benzene ring. This compound typically exhibits properties associated with both aromatic and aliphatic compounds, such as moderate volatility and solubility in organic solvents. The presence of the trifluoromethyl group often imparts unique electronic and steric properties, enhancing its reactivity and potential applications in various chemical reactions, including synthesis and medicinal chemistry. Additionally, the octanoate chain contributes to its hydrophobic characteristics, influencing its behavior in biological systems and its potential use in drug formulation. Overall, this compound's distinctive functional groups suggest it may have applications in fields such as agrochemicals, pharmaceuticals, or materials science, although specific applications would depend on further research into its reactivity and biological activity.
Formula:C17H21F3O3
InChI:InChI=1S/C17H21F3O3/c1-2-23-16(22)8-6-4-3-5-7-15(21)13-9-11-14(12-10-13)17(18,19)20/h9-12H,2-8H2,1H3
InChI key:InChIKey=YONPICYULMSXTP-UHFFFAOYSA-N
SMILES:C(CCCCCCC(OCC)=O)(=O)C1=CC=C(C(F)(F)F)C=C1
Synonyms:
  • Benzeneoctanoic acid, η-oxo-4-(trifluoromethyl)-, ethyl ester
  • Ethyl η-oxo-4-(trifluoromethyl)benzeneoctanoate
  • Ethyl 7-[4-(trifluoromethyl)benzoyl]heptanoate
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