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CAS 930303-82-5

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5-Methylthiophene-3-boronic acid

Description:
5-Methylthiophene-3-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a methylthiophene ring. This compound typically exhibits a molecular structure that includes a five-membered thiophene ring, which contributes to its aromatic properties and potential reactivity. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the methyl group enhances the electron-donating characteristics of the thiophene ring, potentially influencing its reactivity and solubility. Additionally, 5-Methylthiophene-3-boronic acid can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is widely used in the formation of carbon-carbon bonds. Overall, this compound is significant in the development of pharmaceuticals and advanced materials due to its unique structural features and reactivity.
Formula:C5H7BO2S
Synonyms:
  • 5-Methylthiophene-3-boronic acid
  • Boronic acid, B-(5-methyl-3-thienyl)-
  • (5-Methylthiophen-3-yl)boronicacid
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