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CAS 2239305-86-1

:

(3-Chloro-4-methanesulfonylphenyl)boronic acid

Description:
(3-Chloro-4-methanesulfonylphenyl)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 and is widely used in organic synthesis and medicinal chemistry. This compound features a chlorinated aromatic ring, which enhances its reactivity and potential for substitution reactions. The methanesulfonyl group contributes to its solubility and stability in various solvents, making it suitable for diverse applications. The boronic acid moiety allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, the presence of the chlorine atom can influence the electronic properties of the molecule, potentially affecting its reactivity and interactions with biological targets. Overall, (3-Chloro-4-methanesulfonylphenyl)boronic acid is a versatile compound with significant implications in synthetic organic chemistry and drug development.
Formula:C7H8BClO4S
Synonyms:
  • (3-Chloro-4-methanesulfonylphenyl)boronic acid
  • Boronic acid, B-[3-chloro-4-(methylsulfonyl)phenyl]-
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