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CAS 468718-30-1

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5-Cyano-2-fluorophenylboronic acid

Description:
5-Cyano-2-fluorophenylboronic 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. This compound features a cyano group (-CN) and a fluorine atom (-F) attached to a phenyl ring, which can influence its reactivity and solubility. The cyano group contributes to the electron-withdrawing properties, enhancing the acidity of the boronic acid, while the fluorine atom can affect the compound's electronic properties and lipophilicity. Typically, boronic acids like this one are utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the presence of both cyano and fluorine substituents may impart unique biological activity, making it a candidate for further investigation in pharmaceutical research. Overall, 5-Cyano-2-fluorophenylboronic acid is a versatile compound with significant potential in synthetic and medicinal chemistry.
Formula:C7H5BFNO2
InChI:InChI=1/C7H5BFNO2/c9-7-2-1-5(4-10)3-6(7)8(11)12/h1-3,11-12H
SMILES:c1cc(c(cc1C#N)B(O)O)F
Synonyms:
  • 5-Cyano-2-fluorobenzeneboronic acid
  • 5-Cyano-2-fluorophenylboronci acid
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