Thiophosgene
Chemical compound / From Wikipedia, the free encyclopedia
Dear Wikiwand AI, let's keep it short by simply answering these key questions:
Can you list the top facts and stats about Thiophosgene?
Summarize this article for a 10 year old
SHOW ALL QUESTIONS
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]
Quick Facts Names, Identifiers ...
| |||
Names | |||
---|---|---|---|
IUPAC name
Carbonothioyl dichloride | |||
Other names
Thiophosgene; Thiocarbonyl chloride; Carbonothioic dichloride | |||
Identifiers | |||
| |||
3D model (JSmol) |
|||
ChEBI | |||
ChemSpider |
| ||
ECHA InfoCard | 100.006.675 | ||
PubChem CID |
|||
RTECS number |
| ||
UNII | |||
CompTox Dashboard (EPA) |
|||
| |||
| |||
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) |
1.558 | ||
Structure | |||
planar, sp2, C2v | |||
Hazards | |||
Occupational safety and health (OHS/OSH): | |||
Main hazards |
Highly toxic | ||
Flash point | 62 °C (144 °F; 335 K) | ||
Related compounds | |||
Related compounds |
| ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Close