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CAS 1072952-25-0

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(2-Fluoro-5-(hydroxymethyl)phenyl)boronicacid

Description:
(2-Fluoro-5-(hydroxymethyl)phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and other nucleophiles. This compound features a fluorine atom at the ortho position relative to the hydroxymethyl group on a phenyl ring, which can influence its reactivity and solubility. The hydroxymethyl group enhances its potential for further functionalization and increases its polarity. Boronic acids are widely used in organic synthesis, particularly in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds. The presence of the fluorine atom may also impart unique electronic properties, potentially affecting the compound's reactivity and interaction with biological systems. Additionally, the compound's solubility in various solvents can be influenced by the functional groups present, making it versatile for applications in medicinal chemistry and materials science. Overall, (2-Fluoro-5-(hydroxymethyl)phenyl)boronic acid is a valuable building block in synthetic organic chemistry.
Formula:C7H8BFO3
InChI:InChI=1S/C7H8BFO3/c9-7-2-1-5(4-10)3-6(7)8(11)12/h1-3,10-12H,4H2
SMILES:c1cc(c(cc1CO)B(O)O)F
Synonyms:
  • 2-Fluoro-5-Hydroxymethylphenylboronic Acid
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