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About This Item
Empirical Formula (Hill Notation):
CsF
CAS Number:
Molecular Weight:
151.90
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
236-487-3
MDL number:
Assay:
99.9% trace metals basis
InChI key
XJHCXCQVJFPJIK-UHFFFAOYSA-M
InChI
1S/Cs.FH/h;1H/q+1;/p-1
SMILES string
[F-].[Cs+]
assay
99.9% trace metals basis
mp
682 °C (lit.)
density
4.115 g/mL at 25 °C (lit.)
Quality Level
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Related Categories
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 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.
Used in the successful synthesis of a single-crystal Dion-Jacobson phase, CsLaTa2O7, that has applications in photocatalysis and superconductivity.
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
Storage Class
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
S Nelson et al.
Science (New York, N.Y.), 265(5173), 774-777 (1994-08-05)
Neurons in the primary visual cortex of the cat are selectively activated by stimuli with particular orientations. This selectivity can be disrupted by the application of antagonists of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) to a local region of the
E J Devor et al.
Alcohol and alcoholism (Oxford, Oxfordshire). Supplement, 1, 157-160 (1991-01-01)
The stimulated activity of platelet adenylate cyclase (AC) has been shown to be significantly lower among alcoholics compared with controls. In this report we demonstrate that stimulated platelet AC activity is under the control of a single major gene locus.
J Kypr et al.
International journal of biological macromolecules, 13(1), 9-13 (1991-02-01)
Ten DNA fragments containing self-complementary alternating sequences of adenine and thymine differing in length and the starting nucleotide were studied by c.d. spectroscopy. It was found that d(TATATATA) but not d(ATATATAT), d(TATATA), d(CTATATAG) or (dT-dA)20 isomerized into the unusual X-DNA
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