| Weight | 141.535 g/mol |
|---|---|
| Formula | CClNO3S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Chlorosulfonyl isocyanate (1189-71-5)
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- Recent developments in the synthetic uses of chlorosulfonyl isocyanate (Chemical Reviews, 1976)
- Reaction of chlorosulfonyl isocyanate with bridge bi- and tricyclic olefins (Journal of Organic Chemistry, 1968)
- Pyrrole chemistry. XXIII. The cyanation of substituted pyrroles with chlorosulfonyl isocyanate (CSI). New syntheses of pyrrole-3-carbonitriles (Canadian Journal of Chemistry, 1981)
- Reaction of dienes with chlorosulfonyl isocyanate (Journal of Organic Chemistry, 1971)
- Synthesis of 1,2,5-Thiadiazolidines 1,1-dioxides (Cyclosulfamides) Starting from Amino Acids and Chlorosulfonyl Isocyanate (Tetrahedron, 2000)
- Recent Advances in the Chemistry of Chlorosulfonyl Isocyanate (Synthesis, 1986)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(=NS(=O)(=O)Cl)=O
-
InChIKeyWRJWRGBVPUUDLA-UHFFFAOYSA-N
- Pubchem - Chlorosulfonyl isocyanate
- Wikipedia - sulfuryl chloride isocyanate
Chlorosulfonyl isocyanate is the chemical compound ClSO2NCO, known as CSI. This compound is a versatile reagent in organic synthesis.
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diethylsulfamoyl chloride
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isopropyl(methyl)sulfamoyl chloride
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benzyl(methyl)sulfamoyl chloride
(36959-70-3)
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1633-84-7
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(98-10-2)
1 alternate name
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isothiazolidine 1,1-dioxide
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Chlorosulfonyl isocyanate
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