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CAS 4347-31-3

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2-Formylthiophene-3-boronic acid

Description:
2-Formylthiophene-3-boronic acid is an organoboron compound characterized by the presence of both a boronic acid functional group and a thiophene ring with an aldehyde substituent. This compound typically exhibits a pale yellow to light brown appearance and is soluble in polar organic solvents due to the presence of the boronic acid group, which can engage in hydrogen bonding. The thiophene ring contributes to its aromatic properties, making it a potential candidate for various applications in organic synthesis and materials science. The boronic acid functionality allows for participation in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds, which is valuable in the synthesis of complex organic molecules. Additionally, the aldehyde group can undergo further reactions, such as reduction or condensation, enhancing its versatility in synthetic chemistry. Overall, 2-Formylthiophene-3-boronic acid is a significant compound in the field of organic chemistry, particularly in the development of pharmaceuticals and advanced materials.
Formula:C5H5BO3S
InChI:InChI=1/C5H5BO3S/c7-3-5-4(6(8)9)1-2-10-5/h1-3,8-9H
SMILES:c1csc(C=O)c1B(O)O
Synonyms:
  • 3-Boronothiophene-2-carboxaldehyde
  • (2-Formyl-3-thienyl)boronic acid
  • (2-Formylthiophen-3-Yl)Boronic Acid
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