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CAS 58416-04-9

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2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, dimethyl ester

Description:
2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, dimethyl ester, with the CAS number 58416-04-9, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic ring containing sulfur. This compound features two carboxylic acid groups that are esterified with methanol, resulting in dimethyl ester functionality. The presence of hydroxyl groups at the 3 and 4 positions of the thiophene ring contributes to its potential for hydrogen bonding and increases its polarity. This compound is likely to exhibit properties typical of both thiophenes and carboxylic acids, such as moderate solubility in polar solvents and potential reactivity in various chemical reactions, including esterification and oxidation. Its structural features suggest potential applications in organic synthesis, materials science, and possibly in the development of pharmaceuticals or agrochemicals due to the bioactivity often associated with thiophene derivatives. However, specific applications and reactivity would depend on further studies and context within chemical research.
Formula:C8H8O6S
InChI:InChI=1/C8H8O6S/c1-13-7(11)5-3(9)4(10)6(15-5)8(12)14-2/h9-10H,1-2H3
InChI key:ZZVINKJCOXPIKL-UHFFFAOYSA-N
SMILES:COC(=O)c1c(c(c(C(=O)OC)s1)O)O
Synonyms:
  • Dimethyl 3,4-dihydroxythiophene-2,5-dicarboxylate
  • 3,4-Dihydroxy-2,5-dicarboxythiophene dimethyl ester
  • 3,4-Dihydroxy-thiophene-2,5-dicarboxylic acid dimethyl ester
  • 3,4-Dihydroxythiophene-2,5-dicarboxylic acid diethyl ester
  • (2E,5E)-2,5-bis[hydroxy(methoxy)methylidene]thiophene-3,4(2H,5H)-dione
  • 3,4-Dihydroxy-thiophene-2,5-dicarboxylicaciddimethyl ester
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