289345
Cesium fluoride
99.9% trace metals basis
Synonyme(s) :
NSC 84270
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A propos de cet article
Formule empirique (notation de Hill) :
CsF
Numéro CAS:
Poids moléculaire :
151.90
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
236-487-3
MDL number:
Assay:
99.9% trace metals basis
Service technique
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Laissez-nous vous aiderQuality Level
assay
99.9% trace metals basis
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
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.
Used as a base in a Suzuki cross-coupling synthesis of ortho-substituted biaryls. Also employed as a reagent for nucleophilic fluorination of primary halides and sulfonates in protic media such as tert-butyl and tert-pentyl alcohols.
signalword
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
Classe de stockage
11 - 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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Journal of Organometallic Chemistry, 691, 5688-5688 (2006)
Dong Wook Kim et al.
Journal of the American Chemical Society, 128(50), 16394-16397 (2006-12-15)
Aprotic solvents are usually preferred for the SN2 reactions, because nucleophilicity and hence SN2 reactivity are severely retarded by the influence of the partial positive charge of protic solvents. In this work, we introduce a remarkable effect of using tertiary
Katsushi Kitahara et al.
Organic letters, 10(11), 2259-2261 (2008-05-01)
A variety of oximes were synthesized from the corresponding alcohols, alkyl halides, or alkyl sulfonates without using external oxidants. With this simple two-step procedure involving substitution with readily available TsNHOTBS and subsequent treatment with CsF, a range of oximes were