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Merck

198323

Cesium fluoride

99%

Sinónimos:

NSC 84270

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Fórmula empírica (notación de Hill):
CsF
Número CAS:
Peso molecular:
151.90
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
236-487-3
MDL number:
Assay:
99%
Form:
liquid
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Quality Level

assay

99%

form

liquid

mp

682 °C (lit.)

density

4.115 g/mL at 25 °C (lit.)

SMILES string

[F-].[Cs+]

InChI

1S/Cs.FH/h;1H/q+1;/p-1

InChI key

XJHCXCQVJFPJIK-UHFFFAOYSA-M

General description

Cesium fluoride is an inorganic compound known to be a source of fluoride ion and a catalyst in organic synthesis. It has been used in many organic reactions like 1,4−elimination, desilylation, transesterification, acylation, nucleophilic aromatic substitution, etherification, cross−coupling reactions and so on.

Application

Reactant for:
  • Preparation of building blocks for synthesis of fluoroallylic compounds
  • Synthesis of alcohols via hydrolysis of alkyl silyl ethers at neutral pH in buffered mixed organic-aqueous solutions
  • Nucleophilic fluorination of alkynyliodonium salts to form fluorovinylic compounds
  • Nucleophilic aromatic substitution (SNAr) reactions
Used in the successful synthesis of a single-crystal Dion-Jacobson phase, CsLaTa2O7, that has applications in photocatalysis and superconductivity.
Cesium fluoride can be used as:
  • A base in the Suzuki cross-coupling synthesis of ortho-substituted biaryls.
  • A reagent for the nucleophilic fluorination of primary halides and sulfonates in protic media such as tert-butyl and tert-pentyl alcohols.



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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Repr. 2 - STOT RE 2

target_organs

Kidney,Adrenal gland

supp_hazards

Clase de almacenamiento

13 - Non Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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Cesium Fluoride
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2007)
A cesium fluoride promoted efficient and rapid multicomponent synthesis of functionalized 2-amino-3-cyano-4H-pyran and spirooxindole derivatives
Wagh YB, et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 26(10), 1273-1277 (2015)
A new class of SN2 reactions catalyzed by protic solvents: facile fluorination for isotopic labeling of diagnostic molecules
Kim DW, et al.
Journal of the American Chemical Society, 128(50), 16394-16397 (2006)