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CAS 259209-17-1

:

B-(2-Hydroxy-3-methoxyphenyl)boronic acid

Description:
B-(2-Hydroxy-3-methoxyphenyl)boronic acid, with the CAS number 259209-17-1, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenolic structure. This compound features a hydroxyl group and a methoxy group on the aromatic ring, which contribute to its chemical reactivity and solubility properties. Boronic acids are known for their ability to form reversible complexes with diols, making them useful in various applications, including organic synthesis and medicinal chemistry. The presence of the methoxy group enhances the electron-donating character of the aromatic system, potentially influencing its reactivity in cross-coupling reactions, such as Suzuki coupling. Additionally, the hydroxyl group can participate in hydrogen bonding, affecting the compound's solubility in polar solvents. Overall, B-(2-Hydroxy-3-methoxyphenyl)boronic acid is a versatile compound with significant implications in synthetic organic chemistry and materials science.
Formula:C7H9BO4
InChI:InChI=1S/C7H9BO4/c1-12-6-4-2-3-5(7(6)9)8(10)11/h2-4,9-11H,1H3
InChI key:InChIKey=BTYZWLYIOSFCJX-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(O)C(OC)=CC=C1
Synonyms:
  • (2-Hydroxy-3-methoxyphenyl)boronic acid
  • (2-Hydroxy-3-methoxyphenyl)boronicacid
  • 3-Methoxy-2-hydroxyphenylboronic acid
  • B-(2-Hydroxy-3-methoxyphenyl)boronic acid
  • Boronic acid, (2-hydroxy-3-methoxyphenyl)-
  • Boronicacid, (2-hydroxy-3-methoxyphenyl)- (9CI)
  • Boronic acid, B-(2-hydroxy-3-methoxyphenyl)-
  • [2-hydroxy-3-(Methyloxy)phenyl]boronic acid
  • 2-hydroxy-3-methoxyphenylboronic acid
  • 3-METHOXY-2-HYDROXYPHENYL BORONIC ACID
  • REF DUPL: 3-Methoxy-2-hydroxyphenylboronic acid
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