CAS 78162-58-0
:N,N-Diméthyl imidazole-1-sulfonamide
- 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 :Formule :C5H9N3O2SDegré de pureté :96%Couleur et forme :SolidMasse moléculaire :175.2089N,N-Dimethyl-1H-imidazole-1-sulphonamide
CAS :N,N-Dimethyl-1H-imidazole-1-sulphonamideFormule :C5H9N3O2SDegré de pureté :≥95%Couleur et forme : light yellow solidMasse moléculaire :175.21g/molMedetomidine Impurity 4
CAS :Formule :C5H9N3O2SCouleur et forme :White To Off-White SolidMasse moléculaire :175.21N,N-Dimethyl-1H-imidazole-1-sulfonamide
CAS :Formule :C5H9N3O2SDegré de pureté :>98.0%(GC)Couleur et forme :White to Light yellow to Light orange powder to crystalMasse moléculaire :175.211-(N,N-Dimethylsulfamoyl)-1H-imidazole-15N2
CAS :Produit contrôléApplications 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)Formule :C5H915N2NO2SCouleur et forme :NeatMasse moléculaire :177.1961-(Dimethylsulfamoyl)imidazole
CAS :Formule :C5H9N3O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :175.211-(N,N-Dimethylsulfamoyl)-1H-imidazole
CAS :Produit contrôléApplications 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)Formule :C5H9N3O2SCouleur et forme :NeatMasse moléculaire :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.
Formule :C5H9N3O2SDegré de pureté :Min. 95%Masse moléculaire :175.21 g/mol






