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CAS 380430-60-4

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2-(Methanesulfonylamino)phenylboronic acid pinacol ester

Description:
2-(Methanesulfonylamino)phenylboronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is known for its ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications, particularly in the formation of carbon-carbon bonds. The presence of the methanesulfonylamino group enhances its reactivity and solubility in polar solvents. This compound typically appears as a solid and is often utilized in medicinal chemistry and materials science due to its potential in drug development and as a building block in organic synthesis. Its pinacol ester form provides stability and facilitates handling, while the boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions. The compound's properties, such as melting point, solubility, and reactivity, can vary based on the specific conditions and the presence of other functional groups in a reaction environment. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C13H20BNO4S
InChI:InChI=1/C13H20BNO4S/c1-12(2)13(3,4)19-14(18-12)10-8-6-7-9-11(10)15-20(5,16)17/h6-9,15H,1-5H3
SMILES:CC1(C)C(C)(C)OB(c2ccccc2NS(=O)(=O)C)O1
Synonyms:
  • Methanesulfonamide, N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
  • N-[2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanesulfonamide
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