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CAS 338454-45-8

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B-[5-(Hydroxymethyl)-2-thienyl]boronic acid

Description:
B-[5-(Hydroxymethyl)-2-thienyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a thienyl ring. This compound features a hydroxymethyl substituent on the thienyl ring, which enhances its solubility and reactivity. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis, medicinal chemistry, and materials science. The thienyl moiety contributes to the compound's electronic properties, potentially influencing its reactivity and interactions in chemical reactions. Additionally, the presence of the hydroxymethyl group can facilitate hydrogen bonding and increase the compound's polarity. B-[5-(Hydroxymethyl)-2-thienyl]boronic acid may be utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds, which is essential in the synthesis of complex organic molecules. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their role in developing new materials and pharmaceuticals.
Formula:C5H7BO3S
InChI:InChI=1S/C5H7BO3S/c7-3-4-1-2-5(10-4)6(8)9/h1-2,7-9H,3H2
InChI key:InChIKey=IVBZNXLSUVVBCY-UHFFFAOYSA-N
SMILES:B(O)(O)C=1SC(CO)=CC1
Synonyms:
  • 5-(Hydroxymethyl)-2-Thiophenenboronic Acid
  • 5-(Hydroxymethyl)thiophene-2-boronic acid
  • 5-(Hydroxymethyl)thiophene-2-boronic aicd
  • B-[5-(Hydroxymethyl)-2-thienyl]boronic acid
  • Boronic acid, [5-(hydroxymethyl)-2-thienyl]-
  • [5-(Hydroxymethyl)-2-thienyl]boronic acid
  • [5-(Hydroxymethyl)Thiophen-2-Yl]Boronic Acid
  • boronic acid, B-[5-(hydroxymethyl)-2-thienyl]-
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