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CAS 850568-04-6

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2-Fluoro-5-(methoxycarbonyl)phenylboronic acid

Description:
2-Fluoro-5-(methoxycarbonyl)phenylboronic 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 applications, including organic synthesis and medicinal chemistry. The compound features a fluorine atom at the ortho position relative to the boronic acid group on a phenyl ring, which can influence its reactivity and solubility. The methoxycarbonyl group, a carboxylate derivative, enhances the compound's polarity and can participate in further chemical transformations. This compound is typically used in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Its unique structural features contribute to its potential utility in the development of pharmaceuticals and agrochemicals. Additionally, the presence of both electron-withdrawing and electron-donating groups in its structure can affect its electronic properties, making it a subject of interest in material science and organic electronics.
Formula:C8H8BFO4
InChI:InChI=1/C8H8BFO4/c1-14-8(11)5-2-3-7(10)6(4-5)9(12)13/h2-4,12-13H,1H3
SMILES:COC(=O)c1ccc(c(c1)B(O)O)F
Synonyms:
  • 2-Fluoro-5-(methoxycarbonyl)benzeneboronic acid
  • (2-Fluoro-5-methoxycarbonylphenyl)boronic acid
  • [3-Fluoro-4-(Hydrazinocarbonyl)Phenyl]Boronic Acid
  • 2-Fluoro-5-methoxycarbonylphenylboronicacid
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