CAS 898771-76-1
:ethyl 7-oxo-7-(3-thienyl)heptanoate
Description:
Ethyl 7-oxo-7-(3-thienyl)heptanoate 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 (7-oxo) and a thienyl substituent at the 7-position. The presence of the thienyl group, which is a five-membered aromatic ring containing sulfur, contributes to the compound's unique chemical properties and potential biological activity. Ethyl 7-oxo-7-(3-thienyl)heptanoate may exhibit interesting reactivity due to the combination of the carbonyl and thienyl functionalities, making it a candidate for various synthetic applications in organic chemistry. Its molecular structure suggests potential uses in pharmaceuticals or agrochemicals, although specific applications would depend on further research into its biological activity and interactions. As with many organic compounds, safety and handling precautions should be observed, particularly in laboratory settings.
Formula:C13H18O3S
InChI:InChI=1/C13H18O3S/c1-2-16-13(15)7-5-3-4-6-12(14)11-8-9-17-10-11/h8-10H,2-7H2,1H3
SMILES:CCOC(=O)CCCCCC(=O)c1ccsc1
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