CAS 896618-51-2
:ethyl 3-(thiophene-3-carbonyl)benzoate
Description:
Ethyl 3-(thiophene-3-carbonyl)benzoate is an organic compound characterized by its ester functional group, which is derived from benzoic acid and ethyl alcohol. The presence of a thiophene ring, a five-membered aromatic heterocycle containing sulfur, contributes to its unique chemical properties and potential reactivity. This compound typically exhibits moderate solubility in organic solvents due to its hydrophobic aromatic components, while its polar ester group may enhance interactions with polar solvents. Ethyl 3-(thiophene-3-carbonyl)benzoate may display interesting biological activities, making it a candidate for further research in medicinal chemistry. Its structure suggests potential applications in organic synthesis, particularly in the development of new materials or pharmaceuticals. The compound's stability and reactivity can be influenced by the electronic effects of the thiophene and benzoate moieties, which may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Overall, this compound represents a versatile building block in organic chemistry with potential applications in various fields.
Formula:C14H12O3S
InChI:InChI=1/C14H12O3S/c1-2-17-14(16)11-5-3-4-10(8-11)13(15)12-6-7-18-9-12/h3-9H,2H2,1H3
SMILES:CCOC(=O)c1cccc(c1)C(=O)c1ccsc1
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