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CAS 690632-72-5

:

(5-bromo-2,3-dihydro-1-benzofuran-7-yl)boronic acid

Description:
(5-bromo-2,3-dihydro-1-benzofuran-7-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a benzofuran moiety. This compound features a bromine atom at the 5-position of the benzofuran ring, which contributes to its reactivity and potential applications in organic synthesis. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, including Suzuki coupling reactions for the formation of carbon-carbon bonds. The dihydrobenzofuran structure provides a fused bicyclic system that can influence the compound's physical and chemical properties, such as solubility and stability. Additionally, the presence of the bromine atom can enhance the compound's electrophilicity, making it a valuable intermediate in the synthesis of more complex organic molecules. Overall, this compound is of interest in medicinal chemistry and materials science due to its unique structural features and functional groups.
Formula:C8H8BBrO3
InChI:InChI=1/C8H8BBrO3/c10-6-3-5-1-2-13-8(5)7(4-6)9(11)12/h3-4,11-12H,1-2H2
SMILES:C1COc2c1cc(cc2B(O)O)Br
Synonyms:
  • 5-Bromo-2,3-dihydrobenzo[b]furan-7-boronic Acid
  • (5-Bromo-2,3-dihydrobenzofuran-7-yl)boronicacid
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