CAS 898777-45-2
:ethyl 7-(4-iodophenyl)-7-oxo-heptanoate
Description:
Ethyl 7-(4-iodophenyl)-7-oxo-heptanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of heptanoic acid and ethanol. The presence of a 4-iodophenyl group indicates that the compound has a phenyl ring substituted with an iodine atom, contributing to its unique chemical properties and potential reactivity. The ketone functionality (7-oxo) suggests that there is a carbonyl group (C=O) located at the seventh carbon of the heptanoate chain, which can influence the compound's reactivity and stability. This compound may exhibit interesting biological activities due to the iodine substitution, which can enhance lipophilicity and alter pharmacokinetic properties. Additionally, the heptanoate chain provides a hydrophobic character, which may affect solubility in various solvents. Ethyl 7-(4-iodophenyl)-7-oxo-heptanoate may be of interest in medicinal chemistry and materials science, particularly in the development of pharmaceuticals or agrochemicals. However, specific applications and biological activities would require further investigation.
Formula:C15H19IO3
InChI:InChI=1/C15H19IO3/c1-2-19-15(18)7-5-3-4-6-14(17)12-8-10-13(16)11-9-12/h8-11H,2-7H2,1H3
SMILES:CCOC(=O)CCCCCC(=O)c1ccc(cc1)I
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