CAS 78162-58-0
:N,N-Dimetil imidazol-1-sulfonamida
- 1-(Dimethylsulfamoyl)imidazole
- N,N-dimethyl-1H-imidazole-1-sulfonamide
- Imidazole-1-sulfonic acid dimethylamide
- N,N-Dimethyl-imidazole-1-sulfonamide
N,N-Dimethyl imidazole-1-sulfonamide
CAS:Fórmula:C5H9N3O2SPureza:96%Forma y color:SolidPeso molecular:175.2089N,N-Dimethyl-1H-imidazole-1-sulphonamide
CAS:N,N-Dimethyl-1H-imidazole-1-sulphonamideFórmula:C5H9N3O2SPureza:≥95%Forma y color: light yellow solidPeso molecular:175.21g/molMedetomidine Impurity 4
CAS:Fórmula:C5H9N3O2SForma y color:White To Off-White SolidPeso molecular:175.21N,N-Dimethyl-1H-imidazole-1-sulfonamide
CAS:Fórmula:C5H9N3O2SPureza:>98.0%(GC)Forma y color:White to Light yellow to Light orange powder to crystalPeso molecular:175.211-(N,N-Dimethylsulfamoyl)-1H-imidazole-15N2
CAS:Producto controladoApplications 1-(N,N-Dimethylsulfamoyl)-1H-imidazole-15N2 is a labelled imidazole (I350202) derivative, used in the preparation of Histamine H3 Receptor Agonists and druglike angiotensin II compounds with affinity for the AT2 receptor.
References Wijtmans, M. et al.: J. Med. Chem., 51, 2944 (2008); Georgsson, J. et al.: J. Med. Chem., 50, 1711 (2007)Fórmula:C5H915N2NO2SForma y color:NeatPeso molecular:177.1961-(Dimethylsulfamoyl)imidazole
CAS:Fórmula:C5H9N3O2SPureza:98%Forma y color:SolidPeso molecular:175.211-(N,N-Dimethylsulfamoyl)-1H-imidazole
CAS:Producto controladoApplications 1-(N,N-Dimethylsulfamoyl)-1H-imidazole is an Imidazole (I350200) derivative, used in the preparation of Histamine H3 Receptor Agonists and druglike angiotensin II compounds with affinity for the AT2 receptor.
References Wijtmans, M. et al.: J. Med. Chem., 51, 2944 (2008); Georgsson, J. et al.: J. Med. Chem., 50, 1711 (2007)Fórmula:C5H9N3O2SForma y color:NeatPeso molecular:175.211-(Dimethylsulfamoyl)imidazole
CAS:1-(Dimethylsulfamoyl)imidazole is a chemical compound that belongs to the class of heterocycles. It has been shown to inhibit the activity of two enzymes, which are xanthine oxidase and nitric oxide synthase. 1-(Dimethylsulfamoyl)imidazole is synthesized by reacting 2-aminothiophene with methyl sulfonyl chloride in tetrahydrofuran. The yield of this reaction is low, which may be due to the imidazole ring being a poor nucleophile in this reaction. This chemical has been shown to have an inhibitory potency against xanthine oxidase and nitric oxide synthase, which may be due to its functional groups or dimethylformamide solvate state. The mechanism for 1-(dimethylsulfamoyl)imidazole's inhibition of these enzymes is not yet known.
Fórmula:C5H9N3O2SPureza:Min. 95%Peso molecular:175.21 g/mol






