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CAS 849062-04-0

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B-[2,6-Difluoro-3-(1-methylethoxy)phenyl]boronic acid

Description:
B-[2,6-Difluoro-3-(1-methylethoxy)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, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with two fluorine atoms and an isopropoxy group, which can influence its reactivity and solubility. The difluorophenyl moiety enhances the electronic properties of the compound, potentially increasing its reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling. Additionally, the presence of the boronic acid group allows for the formation of boronate esters, which are valuable intermediates in organic synthesis. This compound may also exhibit interesting biological properties, making it a candidate for further research in drug development. Overall, its unique structure and functional groups contribute to its versatility in chemical applications.
Formula:C9H11BF2O3
InChI:InChI=1S/C9H11BF2O3/c1-5(2)15-7-4-3-6(11)8(9(7)12)10(13)14/h3-5,13-14H,1-2H3
InChI key:InChIKey=YMUAZQJBMFLGEI-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(OC(C)C)=CC=C1F
Synonyms:
  • (2,6-Difluoro-3-isopropoxyphenyl)boronic acid
  • 2,6-Difluoro-3-Isopropoxyphenylboronic Acid
  • B-[2,6-Difluoro-3-(1-methylethoxy)phenyl]boronic acid
  • Boronic acid, B-[2,6-difluoro-3-(1-methylethoxy)phenyl]-
  • Boronic acid, [2,6-difluoro-3-(1-methylethoxy)phenyl]-
  • [2,6-Difluoro-3-(propan-2-yloxy)phenyl]boronic acid
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