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CAS 5576-49-8

:

Methanesulfonamide, N-[4-[2-[(1-methylethyl)amino]acetyl]phenyl]-, hydrochloride (1:1)

Description:
Methanesulfonamide, N-[4-[2-[(1-methylethyl)amino]acetyl]phenyl]-, hydrochloride (1:1), commonly referred to by its CAS number 5576-49-8, is a chemical compound characterized by its sulfonamide structure, which includes a methanesulfonamide group. This compound features a phenyl ring substituted with an acetyl group and an isopropylamino moiety, contributing to its biological activity. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, enhancing its utility in pharmaceutical applications. The presence of the sulfonamide functional group suggests potential antimicrobial properties, while the isopropylamino group may influence its pharmacokinetics and receptor interactions. This compound is often studied for its potential therapeutic effects, particularly in the context of drug development. Its stability, solubility, and reactivity can be influenced by pH and temperature, making it important to consider these factors in experimental settings. Overall, this compound represents a significant interest in medicinal chemistry due to its structural features and potential biological implications.
Formula:C12H18N2O3S·ClH
InChI:InChI=1S/C12H18N2O3S.ClH/c1-9(2)13-8-12(15)10-4-6-11(7-5-10)14-18(3,16)17;/h4-7,9,13-14H,8H2,1-3H3;1H
InChI key:InChIKey=PGJCHLFPMKTGCD-UHFFFAOYSA-N
SMILES:C(CNC(C)C)(=O)C1=CC=C(NS(C)(=O)=O)C=C1.Cl
Synonyms:
  • 4-(2-Isopropylaminoacetyl)phenyl methanesulfonamide Hydrochloride
  • Methanesulfonamide, N-[4-[2-[(1-methylethyl)amino]acetyl]phenyl]-, hydrochloride (1:1)
  • Methanesulfonamide, N-[4-[[(1-methylethyl)amino]acetyl]phenyl]-, monohydrochloride
  • Methanesulfonanilide, 4′-[(isopropylamino)acetyl]-, monohydrochloride
  • N-{4-[N-(propan-2-yl)glycyl]phenyl}methanesulfonamide hydrochloride (1:1)
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