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CAS 850589-56-9

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B-[3-Fluoro-5-(phenylmethoxy)phenyl]boronic acid

Description:
B-[3-Fluoro-5-(phenylmethoxy)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. This compound features a phenyl ring substituted with a methoxy group and a fluorine atom, contributing to its unique electronic properties and potential reactivity. The presence of the boronic acid group allows for applications in cross-coupling reactions, particularly in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The fluorine atom can enhance the compound's lipophilicity and influence its biological activity, while the methoxy group may affect solubility and stability. Overall, this compound is of interest in medicinal chemistry and materials science due to its versatile reactivity and potential applications in drug development and organic synthesis.
Formula:C13H12BFO3
InChI:InChI=1S/C13H12BFO3/c15-12-6-11(14(16)17)7-13(8-12)18-9-10-4-2-1-3-5-10/h1-8,16-17H,9H2
InChI key:InChIKey=QQOFKMPPQQMUDH-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=CC(B(O)O)=CC(F)=C2
Synonyms:
  • (3-Benzyloxy-5-Fluoro)Benzeneboronic Acid
  • (3-Fluoro-5-phenylmethoxyphenyl)boronic acid
  • B-[3-Fluoro-5-(phenylmethoxy)phenyl]boronic acid
  • Boronic acid, B-[3-fluoro-5-(phenylmethoxy)phenyl]-
  • Boronic acid, [3-fluoro-5-(phenylmethoxy)phenyl]-
  • [3-(Benzyloxy)-5-fluorophenyl]boronic acid
  • boronic acid, B-[3-fluoro-5-(phenylmethoxy)phenyl]-3-Benzyloxy-5-Fluorobenzeneboronic Acid
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