Caesium acetate
From Wikipedia, the free encyclopedia
| Caesium acetate[1] | |
|---|---|
|
Caesium acetate |
|
|
Other names
Cesium acetate |
|
| Identifiers | |
| CAS number | 3396-11-0 |
| PubChem | 160687 |
| ChemSpider | 141192 |
| Jmol-3D images | Image 1 |
|
|
|
|
| Properties | |
| Molecular formula | C2H3CsO2 |
| Molar mass | 191.95 g mol−1 |
| Appearance | colourless, hygroscopic |
| Density | 2.423 g/cm3, solid |
| Melting point |
194 °C, 467 K, 381 °F |
| Boiling point |
945 °C, 1218 K, 1733 °F |
| Solubility in water | 945.1 g/100 g (−2.5 °C) 1345.5 g/100 ml (88.5 °C) |
| Hazards | |
| EU Index | not listed |
| Flash point | non-flammable |
| Related compounds | |
| Other anions | Caesium formate |
| Other cations | Lithium acetate Sodium acetate Potassium acetate Rubidium acetate |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
|
| Infobox references | |
Caesium acetate or cesium acetate is an ionic caesium compound with the molecular formula CH3CO2Cs often used in organic synthesis especially in Perkin synthesis; formation of unsaturated cinnamic-type acids by the condensation of aromatic aldehydes with fatty acids.[2]
It may be formed by the reaction of caesium hydroxide or caesium oxide with acetic acid.
[edit] References
- ^ Weast, Robert C., ed. (1981). CRC Handbook of Chemistry and Physics (62nd ed.). Boca Raton, FL: CRC Press. p. B-91. ISBN 0-8493-0462-8..
- ^ Koepp, E.; Vögtle, F. (1987), Synthesis: 177.
[edit] Further reading
- Torisawa, Yasuhiro; Okabe, Hiromitsu; Ikegami, Shiro (1984), "Efficient Inversions of Secondary Alcohols using Cesium Acetate and 18-Crown-6", Chem. Lett. 13 (9): 1555–56, doi:10.1246/cl.1984.1555.
[edit] External links
| This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
|
|||||