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CAS 779331-47-4

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2-Benzyloxy-5-fluorobenzeneboronic acid

Description:
2-Benzyloxy-5-fluorobenzeneboronic acid is an organic 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 substituted on the benzene ring, which can influence its electronic properties and reactivity. The benzyloxy group enhances the solubility and stability of the compound, while also providing a site for further functionalization. This compound is typically used in organic synthesis and medicinal chemistry, where it may serve as an intermediate in the development of pharmaceuticals or agrochemicals. Its boronic acid moiety allows for the formation of boronate esters, which are valuable in the synthesis of complex organic molecules. As with many boronic acids, it is important to handle this compound with care, as it may be sensitive to moisture and air, and should be stored under appropriate conditions to maintain its integrity.
Formula:C13H12BFO3
InChI:InChI=1/C13H12BFO3/c15-11-6-7-13(12(8-11)14(16)17)18-9-10-4-2-1-3-5-10/h1-8,16-17H,9H2
SMILES:c1ccc(cc1)COc1ccc(cc1B(O)O)F
Synonyms:
  • [2-(Benzyloxy)-5-fluorophenyl]boronic acid
  • Boronic acid, B-[5-fluoro-2-(phenylmethoxy)phenyl]-
  • 2-Benzyloxy-5-fluorophenylboronic acid
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