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CAS 20699-85-8

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Methyl 5-amino-1-benzothiophene-2-carboxylate

Description:
Methyl 5-amino-1-benzothiophene-2-carboxylate is an organic compound characterized by its unique structure, which includes a benzothiophene ring fused with a carboxylate group and an amino substituent. This compound typically appears as a solid or crystalline substance and is soluble in organic solvents, reflecting its hydrophobic nature due to the aromatic and thiophene components. The presence of the amino group suggests potential for reactivity, particularly in nucleophilic substitution reactions or as a site for further functionalization. Methyl 5-amino-1-benzothiophene-2-carboxylate may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of compounds with potential therapeutic applications. Its molecular structure allows for various interactions, including hydrogen bonding and π-π stacking, which can influence its behavior in biological systems. As with many organic compounds, safety data should be consulted for handling and usage, as it may pose risks depending on concentration and exposure routes.
Formula:C8H6BrNO2
InChI:InChI=1/C8H6BrNO2/c9-5-1-2-7-6(3-5)10-8(11)4-12-7/h1-3H,4H2,(H,10,11)
SMILES:c1cc2c(cc1Br)N=C(CO2)O
Synonyms:
  • 5-Aminothionaphthene-2-carboxylic acid methyl ester
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