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Names | |||
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IUPAC name
Carbonothioyl dichloride
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Other names
Thiophosgene; Thiocarbonyl chloride; Carbonothioic dichloride
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Identifiers | |||
3D model (JSmol)
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ChEBI | |||
ChemSpider | |||
ECHA InfoCard | 100.006.675 | ||
PubChem CID
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RTECS number |
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UNII | |||
CompTox Dashboard (EPA)
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Properties | |||
CSCl2 | |||
Molar mass | 114.97 g·mol−1 | ||
Appearance | Red liquid | ||
Odor | Persistent, choking odor | ||
Density | 1.50 g/cm3 | ||
Boiling point | 70 to 75 °C (158 to 167 °F; 343 to 348 K) | ||
Decomposes | |||
Solubility in other solvents | Reacts with amines and alcohols, soluble in polar organic solvents | ||
-50.6·10−6 cm3/mol | |||
Refractive index (nD)
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1.558 | ||
Structure | |||
planar, sp2, C2v | |||
Hazards | |||
Occupational safety and health (OHS/OSH): | |||
Main hazards
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Highly toxic | ||
Flash point | 62 °C (144 °F; 335 K) | ||
Related compounds | |||
Related compounds
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Thiophosgene is a red liquid with the formula CSCl2. It is a molecule with trigonal planar geometry. There are two reactive C–Cl bonds that allow it to be used in diverse organic syntheses.[1]