CAS 202658-88-6
:Acetamide, 2-chloro-N-(methylsulfonyl)-
Description:
Acetamide, 2-chloro-N-(methylsulfonyl)-, is an organic compound characterized by its acetamide functional group, which features a carbonyl group (C=O) bonded to a nitrogen atom (N). The presence of a chlorine atom at the 2-position of the acetamide structure introduces a halogen substituent, which can influence the compound's reactivity and polarity. Additionally, the methylsulfonyl group (-SO2CH3) attached to the nitrogen enhances the compound's solubility in polar solvents and may impart unique chemical properties, such as increased stability and potential for nucleophilic substitution reactions. This compound is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its molecular structure suggests that it could exhibit specific biological activities, although detailed studies would be necessary to elucidate its full range of properties and applications. As with many chemical substances, safety data and handling precautions should be observed due to potential toxicity or reactivity.
Formula:C3H6ClNO3S
Synonyms:- N-(chloracetyl)methanesulfonamide
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Found 6 products.
Acetamide, 2-chloro-N-(methylsulfonyl)-
CAS:Formula:C3H6ClNO3SPurity:98%Color and Shape:SolidMolecular weight:171.60262-Chloro-N-(methylsulfonyl)acetamide
CAS:<p>2-Chloro-N-(methylsulfonyl)acetamide</p>Purity:98%Molecular weight:171.60g/mol2-Chloro-N-(methylsulfonyl)acetamide
CAS:Controlled Product<p>Applications 2-Chloro-N-(methylsulfonyl)acetamide acts as a reagent for the preparation of piperazinylquinolonecarboxamides as antivirals. Solid phase preparation of peptidines, glycine-amidine-based oligomers.<br>References Vastl, J., et al.: Chem. Sci., 7, 3317 (2016); Schohe-Loop, R., et al.: PCT Int. Appl. (2006), WO 2006008046 A1 20060126<br></p>Formula:C3H6ClNO3SColor and Shape:NeatMolecular weight:171.6
