[4-(Pyrrolidin-1-ylsulfonyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a pyrrolidin-1-ylsulfonyl group, enhancing its solubility and reactivity. The sulfonyl moiety contributes to the compound's polar nature, making it suitable for various applications in medicinal chemistry and materials science. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, this compound may exhibit biological activity, potentially serving as a pharmacophore in drug development. Its structural characteristics suggest it could interact with biological targets, making it of interest in the field of drug discovery. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.

[4-(pyrrolidin-1-ylsulfonyl)phenyl]boronic acid

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4-(Pyrrolidin-1-ylsulphonyl)benzeneboronic acid

(4-(Pyrrolidin-1-ylsulfonyl)phenyl)boronic acid

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CAS 486422-57-5: [4-(pyrrolidin-1-ylsulfonyl)phenyl]boronic acid

4-(Pyrrolidin-1-ylsulphonyl)benzeneboronic acid

Ref: 54-OR4026

(4-(Pyrrolidin-1-ylsulfonyl)phenyl)boronic acid

Ref: 10-F232221

4-(Pyrrolidinylsulfonyl)phenylboronic acid

Ref: 3D-FP160579

4-(1-PYRROLIDINYLSULFONYL)PHENYLBORONIC ACID

Ref: IN-DA00D9RD