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Merck
CN

20989

氟化铯

BioUltra, ≥99.0% (F)

别名:

NSC 84270

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关于此项目

经验公式（希尔记法）:
CsF
化学文摘社编号:
13400-13-0
分子量:
151.90
NACRES:
NA.25
PubChem Substance ID:
57647888
UNSPSC Code:
12352302
EC Number:
236-487-3
MDL number:
MFCD00010960
Assay:
≥99.0% (F)
Grade:
reagent grade
Solubility:
H2O: 3 M at 20 °C, clear, colorless

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InChI key

XJHCXCQVJFPJIK-UHFFFAOYSA-M

InChI

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

SMILES string

[F-].[Cs+]

grade

reagent grade

product line

BioUltra

assay

≥99.0% (F)

impurities

insoluble matter, passes filter test, ≤0.005% total nitrogen (N)

loss

≤0.5% loss on drying, 110 °C

pH

6.5-7.5 (25 °C, 3 M in H2O)

mp

682 °C (lit.)

solubility

H2O: 3 M at 20 °C, clear, colorless

density

4.115 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): ≤500 mg/kg, sulfate (SO42-): ≤50 mg/kg

cation traces

Al: ≤10 mg/kg, As: ≤0.5 mg/kg, Ba: ≤10 mg/kg, Bi: ≤5 mg/kg, Ca: ≤10 mg/kg, Cd: ≤5 mg/kg, Co: ≤5 mg/kg, Cr: ≤5 mg/kg, Cu: ≤5 mg/kg, Fe: ≤30 mg/kg, K: ≤100 mg/kg, Li: ≤5 mg/kg, Mg: ≤5 mg/kg, Mn: ≤5 mg/kg, Mo: ≤5 mg/kg, Na: ≤50 mg/kg, Ni: ≤5 mg/kg, Pb: ≤5 mg/kg, Sr: ≤5 mg/kg, Zn: ≤5 mg/kg

λ

3 M in H2O

UV absorption

λ: 260 nm Amax: 0.05, λ: 280 nm Amax: 0.05

Quality Level

100

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相关类别

Application

可作为反应物用于：
  • 制备合成氟烯丙基化合物过程中的合成砌块
  • 在中性pH下和缓冲的有机-水混合溶液中，通过水解烷基甲硅烷基醚来合成醇
  • 炔基碘鎓盐的亲核氟化，以形成氟代乙烯基化合物
  • 亲核芳香取代（SNAr）反应
用于成功合成单晶Dion-Jacobson相CsLaTa2O7，其在光催化和超导性方面具有应用。

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

EUH032

存储类别

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCN9982
BCCF2943
BCCC8051
BCBV6109
BCBR1238V

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Jonathan L Sessler et al.
Journal of the American Chemical Society, 130(39), 13162-13166 (2008-09-09)
An ion-pair receptor, 1, containing both cation- and anion-recognizing sites, has been synthesized and characterized. Single-crystal X-ray diffraction structural studies and (1)H NMR spectroscopic analyses confirmed that 1 forms stable 1:1 complexes with CsF in solution and in the solid
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
B Tabakoff et al.
The New England journal of medicine, 318(3), 134-139 (1988-01-21)
Blood platelets are an accessible tissue that reflects the activity of many enzymes found in the brain. To investigate the possible effect on such enzymes of long-term consumption of large quantities of ethanol, we assayed the activities of two enzymes
Tsuyoshi Mita et al.
Organic letters, 13(9), 2354-2357 (2011-04-08)
In the presence of TMSSnBu(3) and CsF, stannylation of N-Boc- and N-Cbz-α-amido sulfones proceeded very well to afford the corresponding α-amido stannanes in moderate-to-high yields. This reaction tolerated α-aryl-, alkenyl-, and alkyl-substituted α-amido sulfones as well as substrates containing either
Timothy Noël et al.
Angewandte Chemie (International ed. in English), 50(38), 8900-8903 (2011-08-13)
[Image: see text] A flow process for Pd-catalyzed carbon fluorine bond formation is described. A microreactor using a packed-bed design allows for easy handling of large quantities of insoluble CsF with precise control over reaction times, efficient mixing, and the
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