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CAS 898758-93-5

:

ethyl 6-(4-methoxy-3-nitro-phenyl)-6-oxo-hexanoate

Description:
Ethyl 6-(4-methoxy-3-nitro-phenyl)-6-oxo-hexanoate is an organic compound characterized by its ester functional group, which is derived from hexanoic acid and ethanol. The presence of a 4-methoxy-3-nitro-phenyl group indicates that the compound has both electron-donating (methoxy) and electron-withdrawing (nitro) substituents, which can influence its reactivity and polarity. The hexanoate chain contributes to the compound's hydrophobic characteristics, while the aromatic ring enhances its stability and potential for various chemical interactions. This compound may exhibit biological activity due to its structural features, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential applications in synthesis and as a precursor for more complex molecules. Additionally, the presence of the nitro group may impart specific reactivity, making it a candidate for further functionalization in organic synthesis. Overall, ethyl 6-(4-methoxy-3-nitro-phenyl)-6-oxo-hexanoate is a versatile compound with potential applications in various fields of chemistry.
Formula:C15H19NO6
InChI:InChI=1/C15H19NO6/c1-3-22-15(18)7-5-4-6-13(17)11-8-9-14(21-2)12(10-11)16(19)20/h8-10H,3-7H2,1-2H3
InChI key:InChIKey=ZXYKLGQSWHLDLV-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(OC)C=CC(C(CCCCC(OCC)=O)=O)=C1
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