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CAS 1375109-01-5

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B-(2-Cyano-5-fluorophenyl)boronic acid

Description:
B-(2-Cyano-5-fluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both a cyano group and a fluorine atom. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar organic solvents. The cyano group contributes to its electronic properties, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in the synthesis of biaryl compounds. The fluorine atom can influence the compound's reactivity and stability, often enhancing its lipophilicity and altering its interaction with biological systems. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug design. Overall, B-(2-Cyano-5-fluorophenyl)boronic acid is a valuable compound in organic synthesis and medicinal chemistry, owing to its unique structural features and reactivity.
Formula:C7H5BFNO2
InChI:InChI=1S/C7H5BFNO2/c9-6-2-1-5(4-10)7(3-6)8(11)12/h1-3,11-12H
InChI key:InChIKey=CAMKHMHTUOCLPU-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C#N)C=CC(F)=C1
Synonyms:
  • B-(2-Cyano-5-fluorophenyl)boronic acid
  • Boronic acid, B-(2-cyano-5-fluorophenyl)-
  • 2-Cyano-5-fluorophenylboronic acid
  • (2-Cyano-5-fluorophenyl)boronic acid
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