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CAS 1333407-14-9

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B-[2-Fluoro-5-(methoxymethyl)phenyl]boronic acid

Description:
B-[2-Fluoro-5-(methoxymethyl)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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a fluorinated phenyl ring, which can influence its electronic properties and reactivity. The methoxymethyl substituent enhances its solubility and stability in organic solvents. This compound is typically used in organic synthesis, medicinal chemistry, and materials science due to its ability to act as a versatile building block in the formation of complex molecules. Additionally, the presence of the boronic acid group allows for potential applications in drug development and the creation of boron-containing materials. Its unique structural features contribute to its reactivity and utility in various chemical processes, making it a valuable compound in research and industrial applications.
Formula:C8H10BFO3
InChI:InChI=1S/C8H10BFO3/c1-13-5-6-2-3-8(10)7(4-6)9(11)12/h2-4,11-12H,5H2,1H3
InChI key:InChIKey=CTPACPLLHKMQDS-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(COC)=CC=C1F
Synonyms:
  • Boronic acid, B-[2-fluoro-5-(methoxymethyl)phenyl]-
  • B-[2-Fluoro-5-(methoxymethyl)phenyl]boronic acid
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