CAS 327189-51-5
:ethyl 6-(4-fluorophenyl)-6-oxohexanoate
Description:
Ethyl 6-(4-fluorophenyl)-6-oxohexanoate, identified by its CAS number 327189-51-5, is an organic compound characterized by its ester functional group and a hexanoate backbone. This compound features a 4-fluorophenyl substituent, which introduces a fluorine atom into the aromatic ring, potentially influencing its reactivity and physical properties. The presence of the keto group (6-oxo) contributes to its chemical behavior, making it a candidate for various synthetic applications, including in pharmaceuticals and agrochemicals. Ethyl 6-(4-fluorophenyl)-6-oxohexanoate is likely to exhibit moderate solubility in organic solvents, while its polar functional groups may impart some degree of hydrophilicity. The compound's structure suggests it may participate in nucleophilic reactions, particularly due to the electrophilic nature of the carbonyl group. Additionally, the fluorine atom can enhance the compound's biological activity and lipophilicity, making it of interest in medicinal chemistry. Overall, this compound's unique structural features position it as a versatile intermediate in organic synthesis.
Formula:C14H17FO3
InChI:InChI=1/C14H17FO3/c1-2-18-14(17)6-4-3-5-13(16)11-7-9-12(15)10-8-11/h7-10H,2-6H2,1H3
SMILES:CCOC(=O)CCCCC(=O)c1ccc(cc1)F
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