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CAS 870718-07-3

:

(3-Benzyloxy-2,6-difluorophenyl)boronic acid

Description:
(3-Benzyloxy-2,6-difluorophenyl)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 applications, including organic synthesis and medicinal chemistry. The compound features a difluorophenyl moiety, which enhances its electronic properties and can influence its reactivity and solubility. The benzyloxy group contributes to the overall stability and lipophilicity of the molecule, potentially improving its bioavailability in pharmaceutical contexts. This compound is typically utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Its unique structure allows for selective reactivity, making it a valuable intermediate in the development of various chemical entities. As with many boronic acids, it is important to handle this compound with care, as it can be sensitive to moisture and air, which may affect its stability and reactivity.
Formula:C13H11BF2O3
InChI:InChI=1/C13H11BF2O3/c15-10-6-7-11(13(16)12(10)14(17)18)19-8-9-4-2-1-3-5-9/h1-7,17-18H,8H2
InChI key:InChIKey=MUKMMBLTLNKOAC-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(F)C(B(O)O)=C(F)C=C2
Synonyms:
  • (3-Benzyloxy-2,6-difluorophenyl)boronic acid
  • B-[2,6-Difluoro-3-(phenylmethoxy)phenyl]boronic acid
  • Boronic acid, B-[2,6-difluoro-3-(phenylmethoxy)phenyl]-
  • Boronic acid, [2,6-difluoro-3-(phenylmethoxy)phenyl]-
  • (2,6-Difluoro-3-phenylmethoxyphenyl)boronic acid
  • 3-(Benzyloxy)-2,6-difluorobenzeneboronic acid
  • 3-(Benzyloxy)-2,6-difluorobenzeneboronicacid97%
  • 3-(Benzyloxy)-2,6-difluorobenzeneboronic acid 97%
  • 3-Benzyloxy-2,6-difluorophenylbornic acid
  • 3-(Benzyloxy)-2
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