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CAS 156635-89-1

:

4-Benzyloxy-2,6-difluorophenylboronicacid

Description:
4-Benzyloxy-2,6-difluorophenylboronic 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, indicating the presence of two fluorine atoms on the aromatic 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 cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds. Its unique structure allows for potential applications in the development of pharmaceuticals and agrochemicals. Additionally, the presence of fluorine atoms can impart desirable characteristics such as increased lipophilicity and metabolic stability. Overall, 4-Benzyloxy-2,6-difluorophenylboronic acid is a versatile compound with significant utility in synthetic organic chemistry.
Formula:C13H11BF2O3
InChI:InChI=1S/C13H11BF2O3/c15-11-6-10(7-12(16)13(11)14(17)18)19-8-9-4-2-1-3-5-9/h1-7,17-18H,8H2
SMILES:c1ccc(cc1)COc1cc(c(c(c1)F)B(O)O)F
Synonyms:
  • 4-Benzyloxy-2,6-difluorophenylboronic acid
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