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Fórmula empírica (notación de Hill):
CsF
Número CAS:
Peso molecular:
151.90
UNSPSC Code:
12352100
MDL number:
NACRES:
NA.21
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Permítanos ayudarleNombre del producto
Cesium Fluoride ChemBeads, NSC 84270
Quality Level
InChI
1S/Cs.FH/h;1H/q+1;/p-1
SMILES string
[F-].[Cs+]
InChI key
XJHCXCQVJFPJIK-UHFFFAOYSA-M
product line
ChemBeads
form
solid
composition
, 14-16 wt. % (loading of base)
Categorías relacionadas
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
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.
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.
For general uses, product is also available in powdered form (198323)
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.
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.
For general uses, product is also available in powdered form (198323)
Features and Benefits
ChemBeads are chemical coated glass beads. ChemBeads offer improved flowability and chemical uniformity perfect for automated solid dispensing and high-throughput experimentation. The method of creating ChemBeads uses no other chemicals or surfactants allowing the user to accurately dispense sub-milligram amounts of chemical.
Other Notes
High-Throughput Reaction Screening with Nanomoles of Solid Reagents Coated on Glass Beads
Versatile Methods to Dispense Sub-Milligram Quantities of Solids using Chemical Coated Beads for High-Throughput Experimentation
ChemBead Enabled High-Throughput Cross-Electrophile Coupling Reveals a New Complementary Ligand
Versatile Methods to Dispense Sub-Milligram Quantities of Solids using Chemical Coated Beads for High-Throughput Experimentation
ChemBead Enabled High-Throughput Cross-Electrophile Coupling Reveals a New Complementary Ligand
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Repr. 2 - STOT RE 2
target_organs
Kidney,Adrenal gland
supp_hazards
Clase de almacenamiento
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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