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CAS 1217500-53-2

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(2-(Benzyloxy)-6-fluorophenyl)boronicacid

Description:
(2-(Benzyloxy)-6-fluorophenyl)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, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a fluorine atom on the phenyl ring, which can influence its electronic properties and reactivity. The benzyloxy group enhances the solubility and stability of the compound, allowing for easier handling in synthetic applications. Typically, boronic acids are utilized in organic synthesis, medicinal chemistry, and materials science due to their versatility in forming carbon-carbon bonds. The presence of the fluorine substituent may also impart unique characteristics such as increased lipophilicity or altered biological activity, making this compound of interest in pharmaceutical research. Overall, (2-(Benzyloxy)-6-fluorophenyl)boronic acid is a valuable building block in the synthesis of complex organic molecules.
Formula:C13H12BFO3
InChI:InChI=1S/C13H12BFO3/c15-11-7-4-8-12(13(11)14(16)17)18-9-10-5-2-1-3-6-10/h1-8,16-17H,9H2
SMILES:c1ccc(cc1)COc1cccc(c1B(O)O)F
Synonyms:
  • 2-Benzyloxy-6-Fluorophenylboronic Acid
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