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CAS 67488-50-0

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3-Thiophenecarboxylic acid, 2,5-dihydro-, methyl ester, 1,1-dioxide

Description:
3-Thiophenecarboxylic acid, 2,5-dihydro-, methyl ester, 1,1-dioxide, commonly referred to as a sulfone derivative of thiophene, exhibits several notable characteristics. This compound features a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur, contributing to its unique chemical properties. The presence of a carboxylic acid moiety, along with a methyl ester functional group, indicates that it can participate in various chemical reactions, including esterification and hydrolysis. The 1,1-dioxide designation suggests that the compound contains sulfone groups, which can enhance its reactivity and solubility in polar solvents. Typically, such compounds may exhibit biological activity, making them of interest in pharmaceutical research. Additionally, the molecular structure may influence its physical properties, such as melting and boiling points, solubility, and stability under different conditions. Overall, this compound's characteristics make it a valuable subject for further study in organic chemistry and materials science.
Formula:C6H8O4S
InChI:InChI=1S/C6H8O4S/c1-10-6(7)5-2-3-11(8,9)4-5/h2H,3-4H2,1H3
InChI key:InChIKey=YHHZABJZHHCDNW-UHFFFAOYSA-N
SMILES:C(OC)(=O)C=1CS(=O)(=O)CC1
Synonyms:
  • 2,5-Dihydro-3-thiophenecarboxylic acid methyl ester 1,1-dioxide
  • 3-Carbomethoxy-3-sulpholene
  • 3-Methoxycarbonyl-3-Sulfolene
  • 3-Thiophenecarboxylic acid, 2,5-dihydro-, methyl ester, 1,1-dioxide
  • Methyl 2,5-Dihydrothiophene-3-Carboxylate 1,1-Dioxide
  • Methyl 2-Methyl-4,5-Dihydrothiophene-3-Carboxylate 1,1-Dioxide
  • Methyl 3-sulfolene-3-carboxylate
  • NSC 640439
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