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CAS 2121513-45-7

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B-(2-Ethoxy-6-fluoro-4-methylphenyl)boronic acid

Description:
B-(2-Ethoxy-6-fluoro-4-methylphenyl)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 chemical reactions, particularly in Suzuki coupling reactions. This compound features a phenyl ring substituted with an ethoxy group, a fluorine atom, and a methyl group, contributing to its unique electronic and steric properties. The presence of the fluorine atom can enhance the compound's reactivity and solubility in organic solvents, while the ethoxy group may improve its stability and solubility in polar environments. Boronic acids are typically used in organic synthesis, medicinal chemistry, and materials science due to their versatility. Additionally, this compound may exhibit specific biological activities, making it of interest in pharmaceutical research. As with many boronic acids, it is essential to handle this substance with care, considering its potential reactivity and the need for appropriate safety measures during use.
Formula:C9H12BFO3
InChI:InChI=1S/C9H12BFO3/c1-3-14-8-5-6(2)4-7(11)9(8)10(12)13/h4-5,12-13H,3H2,1-2H3
InChI key:InChIKey=KYQAQMWBJWTQON-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OCC)C=C(C)C=C1F
Synonyms:
  • B-(2-Ethoxy-6-fluoro-4-methylphenyl)boronic acid
  • Boronic acid, B-(2-ethoxy-6-fluoro-4-methylphenyl)-
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