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CAS 1216665-41-6

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2-Methyl 5-boronobenzo[b]thiophene-2-carboxylate

Description:
2-Methyl 5-boronobenzo[b]thiophene-2-carboxylate is an organic compound characterized by its unique structure, which includes a thiophene ring fused to a benzene-like system, along with a carboxylate group and a boron substituent. The presence of the boron atom typically enhances the compound's reactivity, particularly in cross-coupling reactions, making it valuable in organic synthesis and materials science. The methyl group contributes to the compound's hydrophobic characteristics, influencing its solubility and interaction with other molecules. Additionally, the carboxylate moiety can participate in various chemical reactions, including esterification and nucleophilic attacks. This compound may exhibit interesting electronic properties due to the conjugated system formed by the thiophene and benzene rings, potentially making it useful in applications such as organic electronics, photovoltaics, or as a building block in the synthesis of more complex organic materials. Overall, its structural features suggest a versatile compound with potential applications in both research and industry.
Formula:C10H9BO4S
InChI:InChI=1S/C10H9BO4S/c1-15-10(12)9-5-6-4-7(11(13)14)2-3-8(6)16-9/h2-5,13-14H,1H3
InChI key:InChIKey=LSKRRGSCIAJHMP-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=CC=2C(S1)=CC=C(B(O)O)C2
Synonyms:
  • (2-Methoxycarbonylbenzo[b]thien-5-yl)boronic acid
  • 2-Methyl 5-boronobenzo[b]thiophene-2-carboxylate
  • Benzo[b]thiophene-2-carboxylic acid, 5-borono-, 2-methyl ester
  • [2-(Methoxycarbonyl)-1-benzothiophen-5-yl]boronic acid
  • (2-Methoxycarbonylbenzo[b]thiophen-5-yl)boronic acid
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