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CAS 957060-85-4

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(2-fluoro-4-methylsulfonyl-phenyl)boronic acid

Description:
(2-Fluoro-4-methylsulfonyl-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 applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and a methylsulfonyl group, which can influence its reactivity and solubility. The presence of the boronic acid group imparts acidic properties, allowing it to participate in reactions such as Suzuki coupling, a widely used method for forming carbon-carbon bonds. Additionally, the fluorine and methylsulfonyl substituents can enhance the compound's biological activity and selectivity in pharmaceutical applications. Overall, (2-fluoro-4-methylsulfonyl-phenyl)boronic acid is a versatile compound with significant potential in synthetic chemistry and drug development, owing to its unique structural features and reactivity.
Formula:C7H8BFO4S
InChI:InChI=1/C7H8BFO4S/c1-14(12,13)5-2-3-6(8(10)11)7(9)4-5/h2-4,10-11H,1H3
SMILES:CS(=O)(=O)c1ccc(c(c1)F)B(O)O
Synonyms:
  • 2-Fluoro-4-Methylsulfonylphenylboronic Acid
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