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CAS 915401-97-7

:

[4-(Difluoromethoxy)-3,5-difluorophenyl]boronic acid

Description:
[4-(Difluoromethoxy)-3,5-difluorophenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with difluoromethoxy and difluoro groups. This compound typically exhibits properties such as high reactivity due to the boronic acid moiety, which can participate in various chemical reactions, including Suzuki coupling and other cross-coupling reactions. The difluoromethoxy group enhances its solubility and stability in organic solvents, while the difluoro substitutions can influence its electronic properties and reactivity. The presence of fluorine atoms often imparts unique characteristics, such as increased lipophilicity and altered biological activity. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in various applications, including drug development and materials science. Overall, this compound is of interest in synthetic organic chemistry and medicinal chemistry due to its versatile reactivity and potential applications.
Formula:C7H5BF4O3
InChI:InChI=1/C7H5BF4O3/c9-4-1-3(8(13)14)2-5(10)6(4)15-7(11)12/h1-2,7,13-14H
SMILES:c1c(cc(c(c1F)OC(F)F)F)B(O)O
Synonyms:
  • boronic acid, B-[4-(difluoromethoxy)-3,5-difluorophenyl]-
  • 3,5-Difluoro-4-difluomethoxyphenylboronicacid
  • 3,5-Difluoro-4-difluoromethoxyphenylboronic acid
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