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CAS 216686-60-1

:

ethyl 2-amino-5-benzylthiophene-3-carboxylate

Description:
Ethyl 2-amino-5-benzylthiophene-3-carboxylate is a chemical compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features an ethyl ester functional group, an amino group, and a benzyl substituent, contributing to its diverse chemical reactivity and potential applications in medicinal chemistry. The presence of the amino group suggests it may participate in various nucleophilic reactions, while the carboxylate moiety can engage in esterification or amidation reactions. The benzyl group can enhance lipophilicity, potentially influencing the compound's biological activity and solubility. Ethyl 2-amino-5-benzylthiophene-3-carboxylate may exhibit interesting pharmacological properties, making it a candidate for further research in drug development. Its specific properties, such as melting point, solubility, and reactivity, would typically be determined through experimental methods and may vary based on the conditions under which it is studied. As with many organic compounds, safety data and handling precautions should be considered when working with this substance.
Formula:C14H15NO2S
InChI:InChI=1/C14H15NO2S/c1-2-17-14(16)12-9-11(18-13(12)15)8-10-6-4-3-5-7-10/h3-7,9H,2,8,15H2,1H3
SMILES:CCOC(=O)c1cc(Cc2ccccc2)sc1N
Synonyms:
  • 3-Thiophenecarboxylic Acid, 2-Amino-5-(Phenylmethyl)-, Ethyl Ester
  • Ethyl 2-amino-5-benzylthiophene-3-carboxylate
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