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CAS 957120-73-9

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B-[4-[[(2-Methyl-1-oxopropyl)amino]sulfonyl]phenyl]boronic acid

Description:
B-[4-[[(2-Methyl-1-oxopropyl)amino]sulfonyl]phenyl]boronic acid, with the CAS number 957120-73-9, is a boronic acid derivative characterized by its unique functional groups, which include a boronic acid moiety and a sulfonamide group. This compound typically exhibits properties such as moderate solubility in polar solvents, which is common for boronic acids due to their ability to form hydrogen bonds. The presence of the sulfonamide group enhances its potential for biological activity, making it of interest in medicinal chemistry, particularly in the development of inhibitors for various enzymes. The compound's structure suggests it may participate in reversible covalent bonding with diols, a characteristic feature of boronic acids, which is significant in applications such as drug design and molecular recognition. Additionally, its stability under physiological conditions and potential for selective reactivity make it a valuable candidate for further research in therapeutic applications. Overall, this compound exemplifies the diverse functionalities that boronic acids can offer in chemical and biological contexts.
Formula:C10H14BNO5S
InChI:InChI=1S/C10H14BNO5S/c1-7(2)10(13)12-18(16,17)9-5-3-8(4-6-9)11(14)15/h3-7,14-15H,1-2H3,(H,12,13)
InChI key:InChIKey=ULFYGOKHOJNHLQ-UHFFFAOYSA-N
SMILES:S(NC(C(C)C)=O)(=O)(=O)C1=CC=C(B(O)O)C=C1
Synonyms:
  • B-[4-[[(2-Methyl-1-oxopropyl)amino]sulfonyl]phenyl]boronic acid
  • Boronic acid, B-[4-[[(2-methyl-1-oxopropyl)amino]sulfonyl]phenyl]-
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