Caesium acetate
Caesium acetate | |
---|---|
IUPAC name | Caesium acetate |
Other names | Cesium acetate |
Identifiers | |
InChI | InChI=1/C2H4O2.Cs/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1 |
InChIKey | ZOAIGCHJWKDIPJ-REWHXWOFAB |
Standard InChI | InChI=1S/C2H4O2.Cs/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1 |
Standard InChIKey | ZOAIGCHJWKDIPJ-UHFFFAOYSA-M |
CAS number | [ | ]
EC number | |
ChemSpider | |
PubChem | |
Properties[1] | |
Molecular formula | C2H3CsO2 |
Molar mass | 191.95 g mol−1 |
Appearance | colourless solid |
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 ml (–2.5 °C) 1345.5 g/100 ml (88.5 ºC) |
Hazards | |
EU index number | 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) |
Caesium 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]
References
Further reading
- Torisawa, Yasuhiro; Okabe, Hiromitsu; Ikegami, Shiro Efficient Inversions of Secondary Alcohols using Cesium Acetate and 18-Crown-6. Chem. Lett. 1984, 13 (9), 1555–56. DOI: 10.1246/cl.1984.1555.
External links
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