CAS 122115-52-0
:ethyl 7-(4-chlorophenyl)-7-oxoheptanoate
Description:
Ethyl 7-(4-chlorophenyl)-7-oxoheptanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of a carboxylic acid and an alcohol. This compound features a heptanoate backbone, indicating it has a seven-carbon chain, with a ketone group at the seventh position and a 4-chlorophenyl substituent at the same carbon. The presence of the chlorophenyl group suggests potential applications in pharmaceuticals or agrochemicals, as halogenated aromatic compounds often exhibit unique biological activities. The molecular structure contributes to its physical properties, such as solubility and boiling point, which are influenced by the ester and ketone functionalities. Ethyl 7-(4-chlorophenyl)-7-oxoheptanoate may also participate in various chemical reactions, including hydrolysis and transesterification, making it a versatile intermediate in organic synthesis. Its specific characteristics, such as melting point, boiling point, and reactivity, would depend on the molecular interactions and the environment in which it is studied.
Formula:C15H19ClO3
InChI:InChI=1/C15H19ClO3/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)Cl
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