| Weight | 114.984 g/mol |
|---|---|
| Formula | CCl2S |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
THIOPHOSGENE (463-71-8)
Score:
#28 in Physical chemistry
,
#1086 in Physics
,
#3070 in Chemistry
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- The Electron Diffraction Investigation of Phosgene, the Six Chloroethylenes, Thiophosgene, -Methylhydroxylamine and Nitromethane1 (Journal of the American Chemical Society, 1935)
- Photodissociation of thiophosgene (Journal of Chemical Physics, 1977)
- Synthesis and thermolysis of a Diels-Alder adduct of pentacene and thiophosgene (Tetrahedron Letters, 2004)
- Fluorescence from the second excited singlet state of thiophosgene vapour (Chemical Physics Letters, 1974)
- Fluorescence from S2 single vibronic levels in thiophosgene vapor: Quantum yields and quenching effects (Journal of Chemical Physics, 1977)
- Thiophosgene in Organic Synthesis (Synthesis, 1978)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H319: Causes serious eye irritation
Warning Serious eye damage/eye irritation - Category 2A - H335: May cause respiratory irritation
Warning Specific target organ toxicity, single exposure; Respiratory tract irritation - Category 3 -
SMILESC(=S)(Cl)Cl
-
InChIKeyZWZVWGITAAIFPS-UHFFFAOYSA-N
- Pubchem - THIOPHOSGENE
- Wikipedia - thiophosgene
Thiophosgene is a red liquid with the formula CSCl2. It is a molecule with trigonal planar geometry. There are two reactive CCl bonds that allow it to be used in diverse organic syntheses.
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THIOPHOSGENE
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