CAS 26118-68-3
:(2-methylpropyl)sulfamoyl chloride
Description:
(2-Methylpropyl)sulfamoyl chloride, with the CAS number 26118-68-3, is an organic compound characterized by the presence of a sulfamoyl group (-SO2NH2) attached to a 2-methylpropyl group. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and storage conditions. It is known for its reactivity, particularly due to the presence of the sulfonyl chloride functional group, which can readily participate in nucleophilic substitution reactions. This makes it useful in organic synthesis, particularly in the preparation of sulfonamide derivatives and other related compounds. The compound is generally soluble in polar organic solvents, and it may exhibit moderate to high toxicity, necessitating careful handling and appropriate safety measures during use. Additionally, it may react with water, releasing hydrochloric acid and forming the corresponding sulfamoyl derivative. As with many sulfamoyl chlorides, it is important to store this compound in a cool, dry place, away from moisture and incompatible materials.
Formula:C4H10ClNO2S
InChI:InChI=1/C4H10ClNO2S/c1-4(2)3-6-9(5,7)8/h4,6H,3H2,1-2H3
SMILES:CC(C)CNS(=O)(=O)Cl
Synonyms:- Isobutylsulfamyl chloride
- Sulfamoyl Chloride, (2-Methylpropyl)-
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Found 4 products.
Sulfamoyl chloride, N-(2-methylpropyl)-
CAS:Formula:C4H10ClNO2SPurity:98%Color and Shape:LiquidMolecular weight:171.6457ISOBUTYLSULFAMOYL CHLORIDE
CAS:Formula:C4H10ClNO2SPurity:98%Color and Shape:LiquidMolecular weight:171.64Isobutylsulfamoyl chloride
CAS:<p>Isobutylsulfamoyl chloride is a compound that belongs to the class of amide and is used as a reagent in organic synthesis. Isobutylsulfamoyl chloride is an intermediate for the synthesis of oligopeptides and amides, which are important in pharmaceutical chemistry. Isobutylsulfamoyl chloride has been shown to be cardiotoxic in vivo, with a concentration-dependent effect on cardiac muscle cells. The toxicity of this substance may be due to its ability to interfere with the metabolism of other compounds by blocking the activity of secondary amines, such as sulfamic acid, which is involved in neurotransmitter production.</p>Formula:C4H10ClNO2SPurity:Min. 95%Molecular weight:171.65 g/mol



