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CAS 870777-17-6

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B-[2-Fluoro-6-(1-methylethoxy)phenyl]boronic acid

Description:
B-[2-Fluoro-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 useful in various chemical reactions, particularly in organic synthesis and medicinal chemistry. The compound features a fluorinated phenyl ring, which can influence its electronic properties and reactivity. The presence of the 1-methylethoxy group enhances its solubility and stability in organic solvents. This compound is often utilized in the development of pharmaceuticals and agrochemicals, as well as in cross-coupling reactions, such as Suzuki reactions, where it serves as a key building block for the formation of carbon-carbon bonds. Its unique structural features contribute to its potential applications in drug discovery and materials science. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C9H12BFO3
InChI:InChI=1/C9H12BFO3/c1-6(2)14-8-5-3-4-7(11)9(8)10(12)13/h3-6,12-13H,1-2H3
InChI key:InChIKey=WVAMTUDWTJMGSG-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OC(C)C)C=CC=C1F
Synonyms:
  • B-[2-Fluoro-6-(1-methylethoxy)phenyl]boronic acid
  • 2-Fluoro-6-isopropoxyphenylboronic acid
  • Boronic acid, [2-fluoro-6-(1-methylethoxy)phenyl]-
  • Boronic acid, B-[2-fluoro-6-(1-methylethoxy)phenyl]-
  • [2-Fluoro-6-[(propan-2-yl]oxy]phenyl]boronic acid
  • See more synonyms
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