CAS 898777-12-3
:ethyl 5-(2-iodophenyl)-5-oxo-pentanoate
Description:
Ethyl 5-(2-iodophenyl)-5-oxo-pentanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of an alcohol (ethanol) and a carboxylic acid. This compound features a pentanoate backbone, indicating a five-carbon chain with a ketone group at the fifth position, and a phenyl group substituted with an iodine atom at the second position. The presence of the iodine atom suggests potential applications in medicinal chemistry and materials science, as halogenated compounds often exhibit unique reactivity and biological activity. Ethyl 5-(2-iodophenyl)-5-oxo-pentanoate may be synthesized through various organic reactions, including acylation and esterification processes. Its molecular structure contributes to its physical properties, such as solubility and boiling point, which are influenced by the presence of both hydrophobic and polar functional groups. This compound may be of interest in research fields such as drug development or synthetic organic chemistry due to its potential reactivity and the presence of the iodine substituent.
Formula:C13H15IO3
InChI:InChI=1/C13H15IO3/c1-2-17-13(16)9-5-8-12(15)10-6-3-4-7-11(10)14/h3-4,6-7H,2,5,8-9H2,1H3
SMILES:CCOC(=O)CCCC(=O)c1ccccc1I
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