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CAS 882562-39-2

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[1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridin-3-yl]boronic acid

Description:
[1-(p-Tolylsulfonyl)pyrrolo[2,3-b]pyridin-3-yl]boronic acid is a chemical compound characterized by its 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. The compound features a pyrrolo[2,3-b]pyridine core, which contributes to its potential biological activity, particularly in the context of targeting specific enzymes or receptors. The presence of the p-tolylsulfonyl group enhances its solubility and stability, making it suitable for various applications, including drug development. This compound may exhibit properties such as moderate to high polarity due to the sulfonyl group, and it may participate in various chemical reactions, including Suzuki coupling, which is significant in the formation of carbon-carbon bonds. Its unique structure suggests potential applications in the development of pharmaceuticals, particularly in the treatment of diseases where targeted inhibition of specific biological pathways is desired. As with many boronic acids, it may also be sensitive to moisture and require careful handling and storage conditions.
Formula:C14H13BN2O4S
InChI:InChI=1/C14H13BN2O4S/c1-10-4-6-11(7-5-10)22(20,21)17-9-13(15(18)19)12-3-2-8-16-14(12)17/h2-9,18-19H,1H3
SMILES:Cc1ccc(cc1)S(=O)(=O)n1cc(c2cccnc12)B(O)O
Synonyms:
  • 1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-ylboronicacid
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