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CAS 2121511-47-3

:

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

Description:
B-[2,3-Difluoro-6-(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 valuable in various chemical reactions, particularly in Suzuki coupling reactions. This compound features a phenyl ring substituted with two fluorine atoms and an ethoxy group, which can influence its reactivity and solubility. The difluoro substitution can enhance the electronic properties of the molecule, potentially increasing its reactivity in organic synthesis. Boronic acids are typically polar and can exhibit moderate solubility in polar solvents, while the presence of the ethoxy group may improve its solubility in organic solvents. Additionally, the compound's structure suggests potential applications in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and agrochemicals. Overall, B-[2,3-Difluoro-6-(1-methylethoxy)phenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry.
Formula:C9H11BF2O3
InChI:InChI=1S/C9H11BF2O3/c1-5(2)15-7-4-3-6(11)9(12)8(7)10(13)14/h3-5,13-14H,1-2H3
InChI key:InChIKey=RBMPKVJAQZVPLN-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OC(C)C)C=CC(F)=C1F
Synonyms:
  • Boronic acid, B-[2,3-difluoro-6-(1-methylethoxy)phenyl]-
  • B-[2,3-Difluoro-6-(1-methylethoxy)phenyl]boronic acid
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