Thioformaldehyde
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| Names | |||
|---|---|---|---|
| Other names
methanethial | |||
| Identifiers | |||
| 865-36-1 | |||
| 3D model (Jmol) | Interactive image | ||
| ChemSpider | 71446 | ||
| EC Number | 200-454-1 | ||
| PubChem | 79115 | ||
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| Properties | |||
| CH2S | |||
| Molar mass | 46.09 | ||
| Appearance | elusive | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
| Infobox references | |||
Thioformaldehyde is the organosulfur compound with the formula CH2S. This compound is very rarely observed because it oligomerizes to 1,3,5-trithiane, which is a stable colorless compound with the same formula. Despite its instability under normal terrestrial conditions, the molecule has been observed in the interstellar medium[1] and has attracted much attention for its fundamental nature.[2] The tendency of thioformaldehyde to form chains and rings is a manifestation of the Double bond rule.
References
- ↑ Despois, D., "Radio Line Observations of Molecular and Isotopic Species in Comet C/1995 O1 (Hale-Bopp) Implications on the Interstellar Origin of Cometary Ices", Earth, Moon, Planets 1999, 79, 103-124.
- ↑ Clouthier, D. J.; Ramsay, D. A., "The Spectroscopy of Formaldehyde and Thioformaldehyde", Annual Review of Physical Chemistry 1983, 34, 31-58. doi:10.1146/annurev.pc.34.100183.000335
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