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Sigma-Aldrich

Silver hexafluoroantimonate(V)

98%

Synonym(s):

Silver hexafluoroantimony, Silver hexafluorostiboranuide

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About This Item

Linear Formula:
AgSbF6
CAS Number:
26042-64-8
Molecular Weight:
343.62
EC Number:
247-429-1
MDL number:
MFCD00003401
UNSPSC Code:
12352302
PubChem Substance ID:
24853650
NACRES:
NA.23

assay

98%

form

powder

reaction suitability

reagent type: catalyst
core: silver

SMILES string

[Ag+].F[Sb-](F)(F)(F)(F)F

InChI

1S/Ag.6FH.Sb/h;6*1H;/q+1;;;;;;;+5/p-6

InChI key

GSXFODUDOAXUBF-UHFFFAOYSA-H

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Application

Generates stable cation radical salts and is used as an acidic catalyst in epoxide opening reactions and sulfenylation reactions. Used to prepare silver 3,3′-dicyanodiphenylacetylene coordination networks for study of the effect of ligands on network structure toward the goal of engineering novel materials.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

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

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Development of a Nazarov cyclization/Wagner-Meerwein rearrangement sequence for the stereoselective synthesis of spirocycles.
Jie Huang et al.
Journal of the American Chemical Society, 129(26), 8060-8061 (2007-06-09)
Chemistry Letters (Jpn), 1901-1901 (1992)
The Journal of Organic Chemistry, 57, 6178-6178 (1992)
Chemistry Letters (Jpn), 1-1 (1993)
Keith A. Hirsch et al.
Inorganic chemistry, 36(14), 2960-2968 (1997-07-02)
Coordination networks of 3,3'-dicyanodiphenylacetylene (3,3'-DCPA, 1) with silver(I) salts characterized by single-crystal X-ray analysis are described. Network topology is found to depend on both the counterion and solvent employed during crystallization. The conformation adopted by the ligand varies between planar

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