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CAS 227305-69-3

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2,3-Dihydrobenzofuran-5-ylboronic acid

Description:
2,3-Dihydrobenzofuran-5-ylboronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a dihydrobenzofuran moiety. This compound typically exhibits properties associated with both the aromatic and boronic acid functionalities, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis and medicinal chemistry. The boronic acid group allows for participation in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds. Additionally, the dihydrobenzofuran structure contributes to its potential biological activity, as many compounds with similar frameworks have been investigated for their pharmacological properties. The compound is likely to be soluble in polar organic solvents and may exhibit moderate stability under standard laboratory conditions. Its reactivity and functional versatility make it a candidate for further research in drug development and materials science.
Formula:C8H9BO3
InChI:InChI=1S/C8H9BO3/c10-9(11)7-1-2-8-6(5-7)3-4-12-8/h1-2,5,10-11H,3-4H2
InChI key:InChIKey=ZIXLJHSFAMVHPC-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C2C(=CC1)OCC2
Synonyms:
  • (2,3-Dihydrobenzo[b]furan-5-yl)boronic acid
  • 2,3-Dihydrobenzo[b]furan-5-boronic acid
  • 2,3-Dihydrobenzofuran-5-Boronic Acid
  • 2,3-Dihydrobenzofuran-5-boronicacid
  • 2,3-Dihydrobenzofuran-5-ylboronic acid
  • Acide 2,3-dihydro-1-benzofur-5-ylboronique
  • B-(2,3-Dihydro-5-benzofuranyl)boronic acid
  • Boronic acid, (2,3-dihydro-5-benzofuranyl)-
  • Boronic acid, B-(2,3-dihydro-5-benzofuranyl)-
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