Interesting facts
Interesting Facts about N-(1-benzyl-3-chloro-2-oxo-propyl)-4-methyl-benzenesulfonamide
N-(1-benzyl-3-chloro-2-oxo-propyl)-4-methyl-benzenesulfonamide is a fascinating compound that showcases the intricate world of organic chemistry. Its unique structure features a sulfonamide group, which has significant implications in biochemistry and medicinal chemistry.
- Pharmaceutical Relevance: Sulfonamides were among the first antibiotics discovered and remain important in various therapeutic applications. This compound could potentially serve as a lead structure for developing new drugs.
- Unique Functional Groups: The presence of both a ketone and a sulfonamide moiety lends to the compound's intriguing reactivity. Such groups can participate in various chemical reactions, making the compound versatile in synthetic pathways.
- Structural Insights: The substituents attached to the benzene ring and the alkyl chain contribute to the compound's biological activity. Scientists often study such modifications to enhance potency and selectivity in drug design.
- Research Potential: Due to its structure, this compound may offer opportunities for further research. Its activity against specific pathogens or its role in inhibiting certain biological pathways could open new avenues in pharmacology.
Furthermore, the intricate balance of functional groups in N-(1-benzyl-3-chloro-2-oxo-propyl)-4-methyl-benzenesulfonamide makes it a prime candidate for studies in structure-activity relationships (SAR). As researchers explore the diverse chemistry surrounding this compound, the ongoing questions regarding its application in medicine and industry continue to inspire innovations in chemical research.
Synonyms
329-30-6
N-(3-Chloro-2-oxo-1-(phenylmethyl)propyl)-4-methylbenzenesulfonamide
n-(4-chloro-3-oxo-1-phenylbutan-2-yl)-4-methylbenzenesulfonamide
1-chloro-3-tosylamido-4-phenyl-2-butanone
Tos-Phe-chloromethylketone
MFCD00000935
NSC 89167
Tosylphenylalanyl chloromethyl ketone, (L)-
SCHEMBL441444
T.P.C.K.
DTXSID20926571
NPE1244
MQUQNUAYKLCRME-UHFFFAOYSA-N
Tosyl-L-phenylalanyl-chloromethane
NSC89167
NSC-89167
AKOS024370910
Benzenesulfonamide, N-(3-chloro-2-oxo-1-(phenylmethyl)propyl)-4-methyl-
Tosyl-L-Phenylalanine chloromethylketone
tosyl-l-phenylalanyl chloromethyl ketone
LS-14569
NCI60_041981
SY075507
NS00043751
(S)-1-Chloro-3-tosylamido-4-phenyl-2-butanone
(S)-1-Chloro-4-phenyl-3-tosylamido-2-butanone
N-(4-Chloro-3-oxo-1-phenylbutan-2-yl)-4-methylbenzene-1-sulfonamide
130021-38-4
Solubility of N-(1-benzyl-3-chloro-2-oxo-propyl)-4-methyl-benzenesulfonamide
The solubility of N-(1-benzyl-3-chloro-2-oxo-propyl)-4-methyl-benzenesulfonamide in various solvents can be quite fascinating and is influenced by several structural components. Here are some key points regarding its solubility:
In summary, while N-(1-benzyl-3-chloro-2-oxo-propyl)-4-methyl-benzenesulfonamide may exhibit some degree of solubility in polar solvents, its overall solubility profile is likely dictated by its complex structure. Understanding the solubility behaviors not only aids in predicting its use in various applications but also informs the development of formulations and delivery methods in medicinal chemistry.