329827
Cesium acetate
99.9% trace metals basis
Sinônimo(s):
Acetic Acid cesium Salt, Cesium Ethanoate
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About This Item
Fórmula linear:
CH3COOCs
Número CAS:
Peso molecular:
191.95
Beilstein:
3595637
Número CE:
Número MDL:
Código UNSPSC:
12352103
ID de substância PubChem:
NACRES:
NA.23
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Ensaio
99.9% trace metals basis
forma
solid
pf
194 °C (lit.)
cadeia de caracteres SMILES
[Cs+].CC([O-])=O
InChI
1S/C2H4O2.Cs/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1
chave InChI
ZOAIGCHJWKDIPJ-UHFFFAOYSA-M
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Aplicação
- 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).
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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Efficient inversions of secondary alcohols using cesium acetate and 18-crown-6.
Torisawa Y, et al.
Chemistry Letters (Jpn), 9, 1555-1556 (1984)
Cesium-modified mesoporous molecular sieves as basic catalysts for Knoevenagel condensations.
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Studies in Surface Science and Catalysis, 125, 367-374 (1999)
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ACS applied materials & interfaces, 12(39), 43967-43975 (2020-09-02)
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A procedure for alcohol inversion using cesium acetate.
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Synthetic Communications, 13(7), 553-557 (1983)
Efficient method for inversion of secondary alcohols by reaction of chloromethanesulfonates with cesium acetate.
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