| Weight | 115.541 g/mol |
|---|---|
| Formula | H2ClNO2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Sulfamoyl chloride (7778-42-9)
7778-42-9
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- Sulfamoyl Chloride, Sulfamides and Sulfimide (Journal of the American Chemical Society, 1962)
- Sulfamoyl-4-oxoquinoline-3-carboxamides: Novel Potentiators of Defective F508-Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Gating. (Bioorganic & Medicinal Chemistry Letters, 2006)
- Hydrolysis of sulfamoyl chlorides. I. Hydrolysis of dimethylsulfamoyl chloride. Heat capacity of activation, the secondary .gamma.-deuterium isotope effect, and solvent isotope effect (Journal of the American Chemical Society, 1972)
- Reinvestigation of the Molecular Structure of N,N-Dimethyl Sulfamoyl Chloride by Electron Diffraction. (Acta Chemica Scandinavica, 1976)
- Chemistry of (triphenylphosphoranylidene)sulfamoyl chloride. I. Reaction with amines and alcohols (Inorganic Chemistry, 1975)
- Chemistry of N-(triphenylphosphoranylidene)sulfamoyl chloride. 2. N-[N-(Triphenylphosphoranylidene)sulfamoyl]-N'-alkylureas and -guanidines (Journal of Chemical & Engineering Data, 1978)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 7778-42-9
-
SMILESNS(=O)(=O)Cl
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InChIKeyQAHVHSLSRLSVGS-UHFFFAOYSA-N
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Most-cited Publications
Safety
Alternate Names
Estimated Properties
| Boiling Point | 568.08 C | EPI Suite |
|---|---|---|
| Melting Point | 244.4 C | EPI Suite |
| Water Solubility | 1e+06 mg/L | EPI Suite |
External Links
Similar Compounds
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Sulfamoyl chloride
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