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CAS 7311-95-7

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Ethyl 2-amino-1-benzothiophene-3-carboxylate

Description:
Ethyl 2-amino-1-benzothiophene-3-carboxylate is an organic compound characterized by its unique structure, which includes a benzothiophene ring fused with an amino group and an ethyl ester functional group. This compound typically appears as a solid or crystalline substance and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its bioactive properties. The presence of the amino group suggests it may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the carboxylate moiety can influence its solubility and reactivity, making it a versatile building block in organic synthesis. Ethyl 2-amino-1-benzothiophene-3-carboxylate may exhibit specific biological activities, which can be explored in drug discovery and development. Safety and handling precautions should be observed, as with any chemical substance, to mitigate risks associated with its use. Overall, this compound represents a significant interest in both academic and industrial research settings.
Formula:C11H11NO2S
InChI:InChI=1/C11H11NO2S/c1-2-14-11(13)9-7-5-3-4-6-8(7)15-10(9)12/h3-6H,2,12H2,1H3
SMILES:CCOC(=O)c1c2ccccc2sc1N
Synonyms:
  • Benzo[b]thiophene-3-carboxylic acid, 2-amino-, ethyl ester
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