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CAS 942589-45-9

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2-Thiophenecarboxylic acid, 3-amino-5-iodo-, methyl ester

Description:
2-Thiophenecarboxylic acid, 3-amino-5-iodo-, methyl ester is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylic acid functional group that has been esterified with methanol, resulting in a methyl ester. The presence of an amino group at the 3-position and an iodine atom at the 5-position of the thiophene ring contributes to its unique reactivity and potential applications in medicinal chemistry and material science. The iodine substituent can enhance the compound's electrophilic properties, making it useful in various chemical reactions, including coupling reactions and as a precursor for further functionalization. Additionally, the compound may exhibit biological activity due to the presence of the amino group, which can participate in hydrogen bonding and other interactions. Overall, this compound's structural features suggest it may have applications in pharmaceuticals or as an intermediate in organic synthesis.
Formula:C6H6INO2S
InChI:InChI=1S/C6H6INO2S/c1-10-6(9)5-3(8)2-4(7)11-5/h2H,8H2,1H3
InChI key:InChIKey=UCHQIMLGNJWRBI-UHFFFAOYSA-N
SMILES:C(OC)(=O)C=1SC(I)=CC1N
Synonyms:
  • 2-Thiophenecarboxylic acid, 3-amino-5-iodo-, methyl ester
  • Methyl 3-amino-5-iodo-2-thiophenecarboxylate
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