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CAS 1217501-48-8

:

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

Description:
B-[2-Methyl-4-[[(1-methylethyl)amino]sulfonyl]phenyl]boronic acid, identified by its CAS number 1217501-48-8, is a boronic acid derivative characterized by its unique functional groups that include a sulfonamide and a boronic acid moiety. This compound typically exhibits properties such as moderate solubility in polar solvents, which is influenced by the presence of the sulfonamide group. The boronic acid functionality allows it to participate in reversible covalent bonding with diols, making it useful in various applications, including medicinal chemistry and organic synthesis. The presence of the isopropylamino group contributes to its potential biological activity, possibly enhancing its interaction with biological targets. Additionally, the compound may exhibit specific reactivity patterns due to the electron-donating and withdrawing effects of its substituents, which can influence its stability and reactivity in different chemical environments. Overall, this compound is of interest in research areas such as drug development and materials science due to its unique structural features and reactivity.
Formula:C10H16BNO4S
InChI:InChI=1S/C10H16BNO4S/c1-7(2)12-17(15,16)9-4-5-10(11(13)14)8(3)6-9/h4-7,12-14H,1-3H3
InChI key:InChIKey=WTJJGVBICYULNX-UHFFFAOYSA-N
SMILES:S(NC(C)C)(=O)(=O)C1=CC(C)=C(B(O)O)C=C1
Synonyms:
  • (4-(N-Isopropylsulfamoyl)-2-methylphenyl)boronicacid
  • [2-Methyl-4-[(propan-2-yl)sulfamoyl]phenyl]boronic acid
  • B-[2-Methyl-4-[[(1-methylethyl)amino]sulfonyl]phenyl]boronic acid
  • (4-(N-Isopropylsulfamoyl)-2-methylphenyl)boronic acid
  • Boronic acid, B-[2-methyl-4-[[(1-methylethyl)amino]sulfonyl]phenyl]-
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