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CAS 874219-47-3

:

[5-(tert-butylsulfamoyl)-2-methyl-phenyl]boronic acid

Description:
[5-(tert-butylsulfamoyl)-2-methyl-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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a tert-butylsulfamoyl group and a methyl group, contributing to its unique chemical properties and potential biological activity. The tert-butylsulfamoyl moiety enhances solubility and stability, while the boronic acid functionality allows for participation in cross-coupling reactions, which are valuable in organic synthesis and medicinal chemistry. This compound may exhibit specific reactivity patterns due to the steric and electronic effects of its substituents, making it a candidate for applications in drug development and material science. Additionally, its structural characteristics suggest potential interactions with biological targets, warranting further investigation into its pharmacological properties.
Formula:C11H18BNO4S
InChI:InChI=1/C11H18BNO4S/c1-8-5-6-9(7-10(8)12(14)15)18(16,17)13-11(2,3)4/h5-7,13-15H,1-4H3
SMILES:Cc1ccc(cc1B(O)O)S(=O)(=O)NC(C)(C)C
Synonyms:
  • [5-(tert-Butylsulfamoyl)-2-methylphenyl]boronic acid
  • (5-(N-(tert-Butyl)sulfamoyl)-2-methylphenyl)boronicacid
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