CAS 333355-34-3
:ethyl 6-oxo-6-(thiophen-3-yl)hexanoate
Description:
Ethyl 6-oxo-6-(thiophen-3-yl)hexanoate 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 hexanoate backbone, indicating a six-carbon chain with a ketone group at the sixth position, contributing to its reactivity and potential applications in organic synthesis. The presence of a thiophene ring, a five-membered aromatic heterocycle containing sulfur, adds to its structural complexity and may impart unique electronic properties, making it of interest in materials science and pharmaceuticals. Ethyl 6-oxo-6-(thiophen-3-yl)hexanoate is likely to exhibit moderate solubility in organic solvents and may participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions, due to the electrophilic nature of the carbonyl group. Its specific properties, such as boiling point, melting point, and reactivity, would depend on the molecular interactions and the environment in which it is studied. Overall, this compound represents a versatile building block in synthetic organic chemistry.
Formula:C12H16O3S
InChI:InChI=1/C12H16O3S/c1-2-15-12(14)6-4-3-5-11(13)10-7-8-16-9-10/h7-9H,2-6H2,1H3
SMILES:CCOC(=O)CCCCC(=O)c1ccsc1
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