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CAS 1401165-15-8

:

B-(4,4-Difluoro-1-cyclohexen-1-yl)boronic acid

Description:
B-(4,4-Difluoro-1-cyclohexen-1-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in various organic transformations, particularly in Suzuki coupling reactions. This compound features a cyclohexene ring substituted with two fluorine atoms at the para position, enhancing its electronic properties and potentially influencing its reactivity. The boronic acid moiety allows for the formation of stable complexes with diols and other Lewis bases, making it useful in synthetic chemistry. Additionally, the difluorinated cyclohexene structure may impart unique steric and electronic characteristics, which can affect its behavior in chemical reactions and interactions with biological systems. The compound is typically handled with care due to the potential reactivity of boronic acids and the presence of fluorine, which can introduce toxicity concerns. Overall, B-(4,4-Difluoro-1-cyclohexen-1-yl)boronic acid is a valuable building block in organic synthesis and materials science.
Formula:C6H9BF2O2
InChI:InChI=1S/C6H9BF2O2/c8-6(9)3-1-5(2-4-6)7(10)11/h1,10-11H,2-4H2
InChI key:InChIKey=UBVNILVKTTUUJH-UHFFFAOYSA-N
SMILES:B(O)(O)C=1CCC(F)(F)CC1
Synonyms:
  • 4,4-Difluorocyclohex-1-enylboronic acid
  • Boronic acid, B-(4,4-difluoro-1-cyclohexen-1-yl)-
  • B-(4,4-Difluoro-1-cyclohexen-1-yl)boronic acid
  • (4,4-Difluorocyclohex-1-en-1-yl)boronic acid
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