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CAS 848779-87-3

:

(2-Benzyloxy-4-fluorophenyl)boronic acid

Description:
(2-Benzyloxy-4-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. This compound features a fluorine atom and a benzyloxy group attached to a phenyl ring, contributing to its unique reactivity and solubility properties. The presence of the fluorine atom can enhance the electronic properties of the molecule, potentially influencing its reactivity and interactions in organic synthesis. Additionally, the boronic acid moiety allows for participation in cross-coupling reactions, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its structural characteristics also suggest potential applications in materials science and catalysis. As with many boronic acids, it is important to handle this compound with care, as it may exhibit sensitivity to moisture and air, which can affect its stability and reactivity.
Formula:C13H12BFO3
InChI:InChI=1S/C13H12BFO3/c15-11-6-7-12(14(16)17)13(8-11)18-9-10-4-2-1-3-5-10/h1-8,16-17H,9H2
InChI key:InChIKey=IFPQNCKVOQKEIU-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(B(O)O)C=CC(F)=C2
Synonyms:
  • (4-Fluoro-2-phenylmethoxyphenyl)boronic acid
  • B-[4-Fluoro-2-(phenylmethoxy)phenyl]boronic acid
  • Boronic acid, B-[4-fluoro-2-(phenylmethoxy)phenyl]-
  • Boronic acid, [4-fluoro-2-(phenylmethoxy)phenyl]-
  • [2-(Benzyloxy)-4-fluorophenyl]boronic acid
  • (2-Benzyloxy-4-fluorophenyl)boronic acid
  • 2-BENZYLOXY-4-FLUOROBENZENEBORONIC ACID
  • 2-BENZYLOXY-4-FLUOROPHENYLBORONIC ACID
  • AKOS BRN-0217
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