Produktname:N-[3-(5-Amino-1,3,4-thiadiazol-2-yl)propyl]-4-methylbenzenesulfonamide

IUPAC Name:N-[3-(5-amino-1,3,4-thiadiazol-2-yl)propyl]-4-methylbenzene-1-sulfonamide

CAS:1199216-00-6
Molekulare Formel:C12H16N4O2S2
Reinheit:95%
Katalognummer:CM664453
Molekulargewicht:312.41

Packungseinheit Verfügbarer Vorrat Preis($) Menge

Nur für den Einsatz in Forschung und Entwicklung..

Anfrage-Formular

   refresh    

Produkt-Details

CAS-Nr.:1199216-00-6
Molekulare Formel:C12H16N4O2S2
Schmelzpunkt:-
SMILES-Code:CC1=CC=C(C=C1)S(=O)(=O)NCCCC1=NN=C(N)S1
Dichte:
Katalognummer:CM664453
Molekulargewicht:312.41
Siedepunkt:
Mdl-Nr.:MFCD13248730
Lagerung:

Category Infos

Thiadiazoles
Thiadiazoles are a subfamily of azoles. Structurally, they are five-membered heterocyclic compounds containing two nitrogen atoms and one sulfur atom, and two double bonds, forming an aromatic ring. Depending on the relative positions of the heteroatoms, there are four possible structures; these forms do not interconvert and are therefore structural isomers rather than tautomers. These compounds themselves are rarely synthesized and have no particular utility, however, compounds that use them as structural motifs are fairly common in pharmacology.


Product Other Information

Product Overview N-[3-(5-Amino-1,3,4-thiadiazol-2-yl)propyl]-4-methylbenzenesulfonamide, or N-propyl-4-methylbenzenesulfonamide (NPMBS), is an organic compound that has been studied for its potential applications in scientific research. NPMBS is a derivative of the thiadiazole ring system, which is a five-membered heterocyclic compound containing one sulfur and two nitrogen atoms. This compound has been studied for its potential applications in the fields of chemistry, biology, and medicine.
Synthesis and Application N-[3-(5-Amino-1,3,4-thiadiazol-2-yl)propyl]-4-methylbenzenesulfonamide can be synthesized in a two-step process. The first step involves the condensation of 4-methylbenzenesulfonamide with 5-amino-1,3,4-thiadiazole-2-ylpropionic acid in an aqueous solution. The second step involves the reaction of the resulting product with sodium hydroxide in an aqueous solution, which yields N-[3-(5-Amino-1,3,4-thiadiazol-2-yl)propyl]-4-methylbenzenesulfonamide. N-[3-(5-Amino-1,3,4-thiadiazol-2-yl)propyl]-4-methylbenzenesulfonamide has been studied for its potential applications in scientific research. It has been used as a model compound for the study of the structure and properties of thiadiazole systems. N-[3-(5-Amino-1,3,4-thiadiazol-2-yl)propyl]-4-methylbenzenesulfonamide has also been used as a starting material for the synthesis of other thiadiazole derivatives. In addition, N-[3-(5-Amino-1,3,4-thiadiazol-2-yl)propyl]-4-methylbenzenesulfonamide has been studied as a potential inhibitor of the enzyme acetylcholinesterase, which is involved in the regulation of neurotransmission.
Future Directions In the future, more research should be done to further explore the potential applications of N-[3-(5-Amino-1,3,4-thiadiazol-2-yl)propyl]-4-methylbenzenesulfonamide. This could include studying its effects on other enzymes and its potential therapeutic applications for the treatment of neurological disorders. In addition, further research should be done to understand the mechanism of action of N-[3-(5-Amino-1,3,4-thiadiazol-2-yl)propyl]-4-methylbenzenesulfonamide and to identify other potential uses for this compound. Finally, more research should be done to investigate the safety and toxicity of N-[3-(5-Amino-1,3,4-thiadiazol-2-yl)propyl]-4-methylbenzenesulfonamide in order to assess its potential risks and benefits.