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CAS 796061-07-9

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2-(p-Toluenesulfonylamino)benzeneboronic acid pinacol ester

Description:
2-(p-Toluenesulfonylamino)benzeneboronic acid pinacol ester is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring and a pinacol ester group. This compound features a p-toluenesulfonylamino group, which enhances its solubility and reactivity in various chemical reactions, particularly in Suzuki coupling reactions. The pinacol ester moiety contributes to its stability and can facilitate the formation of boronate complexes. Typically, compounds like this exhibit moderate to high polarity due to the presence of the sulfonamide and boronic acid functionalities, making them useful in organic synthesis and medicinal chemistry. They may also demonstrate specific reactivity patterns, such as the ability to form covalent bonds with diols or other nucleophiles. Additionally, the compound's structure suggests potential applications in drug development, particularly in targeting specific biological pathways or as intermediates in the synthesis of more complex molecules. Overall, this compound exemplifies the versatility of boronic acids in organic synthesis and their role in developing new therapeutic agents.
Formula:C19H24BNO4S
InChI:InChI=1/C19H24BNO4S/c1-14-10-12-15(13-11-14)26(22,23)21-17-9-7-6-8-16(17)20-24-18(2,3)19(4,5)25-20/h6-13,21H,1-5H3
SMILES:Cc1ccc(cc1)S(=O)(=O)Nc1ccccc1B1OC(C)(C)C(C)(C)O1
Synonyms:
  • 4-methyl-N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]benzenesulfonamide
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