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CAS 89499-43-4

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Methyl 4-amino-2-thiophenecarboxylate

Description:
Methyl 4-amino-2-thiophenecarboxylate is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amino group (-NH2) and a carboxylate ester group (-COOCH3) attached to the thiophene ring, contributing to its reactivity and potential applications in pharmaceuticals and agrochemicals. The presence of the amino group allows for hydrogen bonding and increases the compound's solubility in polar solvents, while the methyl ester enhances its lipophilicity. Methyl 4-amino-2-thiophenecarboxylate may exhibit biological activity, making it of interest in medicinal chemistry for the development of new therapeutic agents. Its synthesis typically involves the functionalization of thiophene derivatives, and it can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. As with many organic compounds, safety precautions should be taken when handling this substance, as it may pose health risks if ingested or inhaled.
Formula:C6H7NO2S
InChI:InChI=1/C6H7NO2S/c1-9-6(8)5-2-4(7)3-10-5/h2-3H,7H2,1H3
InChI key:InChIKey=HCRQNZWIOUMCOW-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=CC(N)=CS1
Synonyms:
  • 2-Thiophenecarboxylic Acid, 4-Amino-, Methyl Ester
  • 4-Amino-Thiophene-2-Carboxylic Acid Methyl Ester
  • Methyl 4-amino-2-thiophenecarboxylate
  • methyl-4-aminothiophene-2-carboxylate
  • 2-Thiophenecarboxylic acid, 4-amino-, methyl ester, hydrochloride
  • 2-Thiophenecarboxylicacid, 4-aMino-, Methyl ester
  • methyl 4-aminothiophene-2-carboxylate hydrochloride
  • methyl 4-aminothiophene-2
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