CAS 10438-96-7

N-Methylsulfamoyl chloride

Description:

N-Methylsulfamoyl chloride, with the CAS number 10438-96-7, is an organic compound characterized by the presence of a sulfonamide functional group. It features a methyl group attached to the nitrogen atom of the sulfonamide, which contributes to its reactivity and solubility properties. This compound is typically a colorless to pale yellow liquid and is known for its strong electrophilic nature due to the presence of the sulfonyl chloride moiety. It is commonly used as a reagent in organic synthesis, particularly in the preparation of sulfonamides and other nitrogen-containing compounds. N-Methylsulfamoyl chloride is sensitive to moisture and should be handled under anhydrous conditions to prevent hydrolysis, which can lead to the formation of less reactive sulfonamides. Safety precautions are essential when working with this compound, as it can be corrosive and may cause irritation to the skin, eyes, and respiratory system. Proper storage in a cool, dry place, away from incompatible materials, is also recommended to maintain its stability.

Formula: CH₄ClNO₂S

InChI: InChI=1S/CH4ClNO2S/c1-3-6(2,4)5/h3H,1H3

InChI key: InChIKey=UJJUEJRWNWVHCM-UHFFFAOYSA-N

SMILES: S(NC)(Cl)(=O)=O

Synonyms:

• Methylaminosulfonyl chloride
• Methylsulfamyl chloride
• N-Methylaminosulfonyl chloride
• N-Methylsulfamoyl chloride
• Sulfamoyl chloride, N-methyl-
• Sulfamoyl chloride, methyl-

Methylsulfamoyl Chloride

CAS: 10438-96-7

Formula: CH₄ClNO₂S

Purity: 97%

Color and Shape: Liquid

Molecular weight: 129.5660

Ref: IN-DA00359K

Methylsulfamoyl chloride

CAS: 10438-96-7

Methylsulfamoyl chloride

Formula: CH₄ClNO₂S

Purity: 98%

Color and Shape: colourless to light yellow liquid

Molecular weight: 129.57g/mol

Ref: 54-OR964584

METHYLSULFAMOYL CHLORIDE

CAS: 10438-96-7

Purity: 95.0%

Color and Shape: Liquid, Colourless liquid

Molecular weight: 129.55999755859375

Ref: 10-F386868

Mesulfamoyl chloride

CAS: 10438-96-7

Mesulfamoyl chloride is a sulphamic acid derivative that acts as an inhibitor of the enzyme sulphotransferase, which is involved in the conversion of sulphamates to sulphones. It has been used in clinical studies for the treatment of cancer and infectious diseases such as hepatitis. Mesulfamoyl chloride has been shown to be effective against oestrone sulphatase and serine proteases, which are enzymes that can lead to cell proliferation.

Formula: CH₄ClNO₂S

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 129.57 g/mol

Ref: 3D-KAA43896