CAS 78162-58-0
:N,N-Dimethyl imidazole-1-sulfonamide
Description:
N,N-Dimethyl imidazole-1-sulfonamide is an organic compound characterized by its imidazole ring structure, which is a five-membered heterocyclic compound containing two nitrogen atoms. This substance features a sulfonamide functional group, which is known for its antibacterial properties and ability to form hydrogen bonds, enhancing its solubility in polar solvents. The presence of dimethyl groups contributes to its overall stability and influences its reactivity. Typically, compounds like N,N-Dimethyl imidazole-1-sulfonamide are utilized in various chemical applications, including as intermediates in organic synthesis and potentially in pharmaceutical formulations due to their biological activity. The compound is likely to exhibit moderate to high polarity, making it soluble in water and other polar solvents, while its imidazole structure may allow for coordination with metal ions or participation in catalytic processes. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C5H9N3O2S
InChI:InChI=1/C5H9N3O2S/c1-7(2)11(9,10)8-4-3-6-5-8/h3-5H,1-2H3
SMILES:CN(C)S(=O)(=O)n1ccnc1
Synonyms:- 1-(Dimethylsulfamoyl)imidazole
- N,N-dimethyl-1H-imidazole-1-sulfonamide
- Imidazole-1-sulfonic acid dimethylamide
- N,N-Dimethyl-imidazole-1-sulfonamide
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Found 8 products.
N,N-Dimethyl imidazole-1-sulfonamide
CAS:Formula:C5H9N3O2SPurity:96%Color and Shape:SolidMolecular weight:175.2089N,N-Dimethyl-1H-imidazole-1-sulphonamide
CAS:N,N-Dimethyl-1H-imidazole-1-sulphonamideFormula:C5H9N3O2SPurity:≥95%Color and Shape: light yellow solidMolecular weight:175.21g/molMedetomidine Impurity 4
CAS:Formula:C5H9N3O2SColor and Shape:White To Off-White SolidMolecular weight:175.21N,N-Dimethyl-1H-imidazole-1-sulfonamide
CAS:Formula:C5H9N3O2SPurity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:175.211-(N,N-Dimethylsulfamoyl)-1H-imidazole-15N2
CAS:Controlled Product<p>Applications 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.<br>References Wijtmans, M. et al.: J. Med. Chem., 51, 2944 (2008); Georgsson, J. et al.: J. Med. Chem., 50, 1711 (2007)<br></p>Formula:C5H915N2NO2SColor and Shape:NeatMolecular weight:177.1961-(Dimethylsulfamoyl)imidazole
CAS:Formula:C5H9N3O2SPurity:98%Color and Shape:SolidMolecular weight:175.211-(N,N-Dimethylsulfamoyl)-1H-imidazole
CAS:Controlled Product<p>Applications 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.<br>References Wijtmans, M. et al.: J. Med. Chem., 51, 2944 (2008); Georgsson, J. et al.: J. Med. Chem., 50, 1711 (2007)<br></p>Formula:C5H9N3O2SColor and Shape:NeatMolecular weight:175.211-(Dimethylsulfamoyl)imidazole
CAS:<p>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.</p>Formula:C5H9N3O2SPurity:Min. 95%Molecular weight:175.21 g/mol






