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CAS 871329-74-7

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(2-methyl-5-morpholinosulfonyl-phenyl)boronic acid

Description:
(2-Methyl-5-morpholinosulfonyl-phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, particularly in medicinal chemistry and organic synthesis. This compound features a phenyl ring substituted with a morpholino group and a sulfonyl moiety, contributing to its unique reactivity and solubility properties. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds. Additionally, the morpholino group enhances the compound's solubility in polar solvents and may influence its biological activity. The compound is typically a white to off-white solid and is handled with standard laboratory precautions due to its potential reactivity. Its applications may extend to drug development, particularly in targeting specific biological pathways or as a building block in the synthesis of more complex molecules.
Formula:C11H16BNO5S
InChI:InChI=1/C11H16BNO5S/c1-9-2-3-10(8-11(9)12(14)15)19(16,17)13-4-6-18-7-5-13/h2-3,8,14-15H,4-7H2,1H3
SMILES:Cc1ccc(cc1B(O)O)S(=O)(=O)N1CCOCC1
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