216674
Silver acetate
ReagentPlus®, 99%
Synonym(s):
Acetic acid silver salt
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All Photos(3)
About This Item
Linear Formula:
CH3COOAg
CAS Number:
Molecular Weight:
166.91
Beilstein:
3595636
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.21
grade:
reagent
form:
powder or chunks
Recommended Products
grade
reagent
Quality Level
product line
ReagentPlus®
Assay
99%
form
powder or chunks
reaction suitability
reagent type: catalyst
core: silver
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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Related Categories
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.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Chemistry of Materials, FL501-FL501 (1999)
Silver acetate-assisted formation of amides from acyl chlorides.
Leggio A, et al.
Tetrahedron Letters, 56(1), 199-202 (2015)
Niels Hadrup et al.
Neurotoxicology, 33(3), 416-423 (2012-04-26)
We compared the neurotoxic effects of 14 nm silver nanoparticles (AgNPs) and ionic silver, in the form of silver acetate (AgAc), in vivo and in vitro. In female rats, we found that AgNPs (4.5 and 9 mg AgNP/kg bw/day) and
M Batt et al.
European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery, 36(2), 182-188 (2008-04-29)
The aim of this study was to evaluate the early and mid term outcome of patients with aortic graft infection who underwent in-situ revascularisation with a silver coated prosthesis. From January 2000 to December 2006, 24 consecutive patients (22 male
Haibo Xie et al.
The Journal of organic chemistry, 75(21), 7468-7471 (2010-10-13)
We described hereby an instance of diastereoselective silver-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with imine compounds. This new method provided synthetically useful, highly substituted tetrahydroimidazole derivatives with efficiency and high diastereoselectivity. We can conveniently obtain fluorinated dihydroimidazole, imidazole, and diamino
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