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Merck
CN

205567

Sigma-Aldrich

Zinc fluoride

powder, 99%

Synonym(s):

Zinc difluoride

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About This Item

Linear Formula:
ZnF2
CAS Number:
Molecular Weight:
103.39
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
Assay:
99%
Form:
powder
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vapor pressure

1 mmHg ( 970 °C)

Assay

99%

form

powder

reaction suitability

reagent type: catalyst
core: zinc

mp

872 °C (lit.)

density

4.95 g/mL at 25 °C (lit.)

SMILES string

F[Zn]F

InChI

1S/2FH.Zn/h2*1H;/q;;+2/p-2

InChI key

BHHYHSUAOQUXJK-UHFFFAOYSA-L

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General description

Zinc fluoride is a Lewis acid catalyst that can be used in a variety of reactions including esterification, Mukaiyama aldol reaction, Mannich reaction, Friedel-Crafts alkylation, and allylation. It can also be used as an additive in numerous catalytic transformations.

Application

Zinc fluoride can be used as a catalyst to synthesize optically active β-amino ketones and esters via asymmetric Mannich reaction.

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Irrit. 2

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

危险化学品
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Zinc Fluoride
Turcotte-Savard M, et al.
e-EROS Encyclopedia of Reagents for Organic Synthesis (2001)
Theoretical studies of valence orbital binding energies in solid zinc sulfide, zinc oxide, and zinc fluoride.
Tossell JA.
Inorganic Chemistry, 16(11), 2944-2949 (1977)
Novel sol-gel prepared zinc fluoride: synthesis, characterisation and acid-base sites analysis.
Guo Y, et al.
Journal of Materials Chemistry, 22(29), 14587-14593 (2009)
J V Embleton et al.
Oral microbiology and immunology, 16(3), 182-184 (2001-05-19)
This study evaluated the ability of topically applied amine fluoride (AmF) and AmF-tin fluoride to inhibit the adhesion of Streptococcus sanguis within a parallel plate flow cell system. One of three AmF compounds and two tin fluoride preparations significantly reduced
Tomoaki Hamada et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 12(4), 1205-1215 (2005-11-04)
Catalytic asymmetric Mannich-type reactions of an alpha-hydrazono ester with silicon enolates in aqueous media have been developed by using ZnF2 and chiral diamines as catalysts. In these reactions, both Zn2+ and a fluoride anion were necessary to achieve high yields

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