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Sigma-Aldrich

Cesium acetate

99.9% trace metals basis

Synonym(s):

Acetic Acid cesium Salt, Cesium Ethanoate

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About This Item

Linear Formula:
CH3COOCs
CAS Number:
Molecular Weight:
191.95
Beilstein/REAXYS Number:
3595637
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

assay

99.9% trace metals basis

form

solid

mp

194 °C (lit.)

SMILES string

[Cs+].CC([O-])=O

InChI

1S/C2H4O2.Cs/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1

InChI key

ZOAIGCHJWKDIPJ-UHFFFAOYSA-M

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Application

  • Tuning diketodioxinone reactivity: biomimetic synthesis of the resorcylate antibiotic fungal metabolites ent-W1278A, -B, and -C, using iterative aromatization reactions.: This study demonstrates the use of cesium acetate in tuning diketodioxinone reactivity for the synthesis of antibiotic fungal metabolites, highlighting its role in iterative aromatization reactions (Navarro et al., 2009).
  • Raman spectroscopy and dioxygen adsorption on Cs-loaded zeolite catalysts for butene isomerization.: The research explores the application of cesium acetate in Cs-loaded zeolite catalysts, demonstrating its effectiveness in butene isomerization through Raman spectroscopy and dioxygen adsorption studies (Li & Davis, 2005).
  • Synthesis of the C3-C19 segment of phorboxazole B.: Cesium acetate is utilized in the complex synthesis of the C3-C19 segment of phorboxazole B, showcasing its importance in advanced organic synthesis processes (Vitale et al., 2005).
  • Beneficial effect of cesium salts on Pd-catalyzed hydroxycarbonylation.: This study reveals the advantageous effects of cesium acetate in palladium-catalyzed hydroxycarbonylation reactions, improving reaction efficiency and product yield (Torisawa et al., 2000).

pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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A procedure for alcohol inversion using cesium acetate.
Huffman JW and Desai RC.
Synthetic Communications, 13(7), 553-557 (1983)
Amée M Buziau et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1155, 122299-122299 (2020-08-24)
The study of the involvement of fructose in the pathogenesis of cardiometabolic disease requires accurate and precise measurements of serum and urinary fructose. The aim of the present study was to develop and validate such a method by Ultra Performance
Modification of kaolinite surfaces with cesium acetate at 25, 120, and 220 C.
Frost RL, et al.
Langmuir, 15(26), 8787-8794 (1999)

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