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CAS 73696-46-5

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2-(benzoylamino)-5-ethylthiophene-3-carboxylic acid

Description:
2-(Benzoylamino)-5-ethylthiophene-3-carboxylic acid is a chemical compound characterized by its unique structure, which includes a thiophene ring substituted with both a benzoylamino group and a carboxylic acid functional group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as stability and potential reactivity due to the presence of the carboxylic acid. The benzoylamino group can enhance the compound's solubility in organic solvents and may influence its biological activity. The ethyl group contributes to the overall hydrophobic character of the molecule. In terms of applications, compounds like this may be explored in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis due to their functional groups that can participate in various chemical reactions. Additionally, the presence of the thiophene moiety may impart interesting electronic properties, making it a candidate for studies in materials science or organic electronics. Overall, this compound's characteristics make it a subject of interest in both synthetic and applied chemistry.
Formula:C14H13NO3S
InChI:InChI=1/C14H13NO3S/c1-2-10-8-11(14(17)18)13(19-10)15-12(16)9-6-4-3-5-7-9/h3-8H,2H2,1H3,(H,15,16)(H,17,18)
SMILES:CCc1cc(c(N=C(c2ccccc2)O)s1)C(=O)O
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