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CAS 886547-94-0

:

1-(Phenylsulfonyl)-7-azaindole-3-boronicacidpinacolester

Description:
1-(Phenylsulfonyl)-7-azaindole-3-boronic acid pinacol ester, identified by its CAS number 886547-94-0, is a chemical compound that features a boronic acid functional group, which is known for its reactivity in forming covalent bonds with diols and its utility in Suzuki coupling reactions. This compound contains a phenylsulfonyl group, which enhances its solubility and stability, and an azaindole moiety, contributing to its potential biological activity. The pinacol ester form indicates that the boronic acid is protected, making it more stable under certain conditions. The compound is likely to exhibit properties typical of boronic acids, such as the ability to participate in various organic synthesis reactions, including cross-coupling reactions. Its unique structure may also suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. However, detailed studies would be necessary to fully elucidate its reactivity, stability, and potential applications in various fields.
Formula:C19H21BN2O4S
InChI:InChI=1S/C19H27BN2O4/c1-12-14-11-13(20-25-18(5,6)19(7,8)26-20)9-10-15(14)22(21-12)16(23)24-17(2,3)4/h9-11H,1-8H3
SMILES:Cc1c2cc(ccc2n(C(=O)OC(C)(C)C)n1)B1OC(C)(C)C(C)(C)O1
Synonyms:
  • 1-(Phenylsulfonyl)-7-Azaindole-3-Boronic Acid Pinacol Ester
  • 1-(Benzenesulfonyl)-1H-Pyrrolo(2,3-B)Pyridine-3-Boronic Acid Pinacol Ester
  • 1-(Benzenesulfonyl)-3-(Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-1H-Pyrrolo[2,3-B]Pyridine
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