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Merck

204374

Sigma-Aldrich

Silver acetate

99.99% trace metals basis

Sinónimos:

Acetic acid silver salt

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About This Item

Fórmula lineal:
CH3COOAg
Número de CAS:
Peso molecular:
166.91
Beilstein/REAXYS Number:
3595636
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

assay

99.99% trace metals basis

form

powder or crystals

reaction suitability

core: silver
reaction type: C-H Activation
reagent type: catalyst

SMILES string

CC(O[Ag])=O

InChI

1S/C2H4O2.Ag/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1

InChI key

CQLFBEKRDQMJLZ-UHFFFAOYSA-M

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Application

Used in a novel preparation of highly reflective, conductive silvered polymer films. Also effectively catalyzes cycloaddition reactions of isocyanoacetates with a variety of olefins.

pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Chemistry of Materials, FL501-FL501 (1999)
Grigg, R. et al.
Tetrahedron, 55, 2025-2025 (1999)
Fabrice Schneider et al.
Annals of vascular surgery, 22(6), 815-821 (2008-10-07)
The primary objective of this study was to compare the efficacy of a collagen silver-coated polyester graft, InterGard, with a gelatin-sealed graft, Gelsoft, both soaked in rifampin, for resistance to direct bacterial contamination in an animal model. The second objective
H Gao et al.
European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery, 39(4), 472-477 (2010-01-12)
To evaluate the efficacy of a silver-coated vascular polyester graft in the prevention of graft infection after inoculation with Staphylococcus aureus in a porcine model. Eighty-four pigs were randomly selected 1:1 to receive a silver-coated or non-silver-coated 8-mm-wide polyester graft
Siddappa Patil et al.
Metallomics : integrated biometal science, 3(1), 74-88 (2010-12-08)
From the reaction of 1-methylimidazole (1a), 4,5-dichloro-1H-imidazole (1b(I)) and 1-methylbenzimidazole (1c) with p-cyanobenzyl bromide (2a), non-symmetrically substituted N-heterocyclic carbene (NHC) [(3a-c)] precursors, 5,6-dimethyl-1H-benzimidazole (1d) and 4,5-diphenyl-1H-imidazole (1e) with p-cyanobenzyl bromide (2a) and benzyl bromide (2b), symmetrically substituted N-heterocyclic carbene (NHC)

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