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CAS 206551-43-1

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5-Acetylthiophene-2-boronic acid

Description:
5-Acetylthiophene-2-boronic acid is an organoboron compound characterized by the presence of both a boronic acid functional group and a thiophene ring. The molecular structure features a thiophene ring substituted at the 2-position with a boronic acid group and at the 5-position with an acetyl group. This compound is typically used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is valuable for forming carbon-carbon bonds. The boronic acid moiety allows for the formation of stable complexes with diols, making it useful in various applications, including drug discovery and materials science. Additionally, the presence of the acetyl group can influence the reactivity and solubility of the compound. 5-Acetylthiophene-2-boronic acid is generally handled with care due to the reactivity of boronic acids, and it is important to store it under appropriate conditions to maintain its stability.
Formula:C6H7BO3S
InChI:InChI=1/C6H7BO3S/c1-4(8)5-2-3-6(11-5)7(9)10/h2-3,9-10H,1H3
SMILES:CC(=O)c1ccc(B(O)O)s1
Synonyms:
  • (5-Acetylthiophen-2-Yl)Boronic Acid
  • 5-Acetyl-2-thiopheneboronic acid
  • 2-Acetylthiphene-2-boronic acid
  • 2-Acetylthiophene-5-Boronic Acid
  • 5-Acetyl-2-thienylboronicAcid
  • 5-Acetylthiophen-2-Ylboronic Acid
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