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CAS 850589-57-0

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(3-fluoro-5-isobutoxy-phenyl)boronic acid

Description:
(3-Fluoro-5-isobutoxy-phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a fluorine atom and an isobutoxy group. The fluorine atom typically enhances the compound's reactivity and can influence its electronic properties, while the isobutoxy group contributes to its solubility and steric hindrance. This compound is likely to exhibit properties typical of boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. Its boronic acid functionality allows for participation in Suzuki-Miyaura cross-coupling reactions, which are vital in the formation of carbon-carbon bonds. Additionally, the presence of the isobutoxy group may affect the compound's stability and reactivity under different conditions. Overall, (3-fluoro-5-isobutoxy-phenyl)boronic acid is a versatile compound with potential applications in drug development and materials science.
Formula:C10H14BFO3
InChI:InChI=1/C10H14BFO3/c1-7(2)6-15-10-4-8(11(13)14)3-9(12)5-10/h3-5,7,13-14H,6H2,1-2H3
SMILES:CC(C)COc1cc(cc(c1)F)B(O)O
Synonyms:
  • (3-Fluoro-5-isobutoxyphenyl)boronic acid
  • boronic acid, B-[3-fluoro-5-(2-methylpropoxy)phenyl]-
  • 3-Fluoro-5-isobutoxyphenylboronicacid
  • 3-Fluoro-5-(Isobutoxy)Benzeneboronic Acid
  • 3-Fluoro-5-isobutoxyphenylboronic acid
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