438448
Silver carbonate
99.999% trace metals basis
Synonym(s):
Disilver carbonate, Silver(I) carbonate
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About This Item
Linear Formula:
Ag2CO3
CAS Number:
Molecular Weight:
275.75
Beilstein:
6936654
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23
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Quality Level
Assay
99.999% trace metals basis
form
powder
reaction suitability
reagent type: catalyst
core: silver
mp
210 °C (dec.) (lit.)
density
6.08 g/mL at 25 °C (lit.)
SMILES string
[Ag]OC(=O)O[Ag]
InChI
1S/CH2O3.2Ag/c2-1(3)4;;/h(H2,2,3,4);;/q;2*+1/p-2
InChI key
KQTXIZHBFFWWFW-UHFFFAOYSA-L
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Application
Silver carbonate is used in Koenigs-Knorr glycosylation. The product is used as a protective agent to prevent the sedimentation of silver nanoparticles (AgNPs).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Photocatalytic behavior and photo-corrosion of visible-light-active silver carbonate/titanium dioxide.
Wang Y, et al.
Materials Letters, 115, 85-88 (2014)
Silver carbonate and stability in colloidal silver: a by-product of the electric spark discharge method.
Tseng KH, et al.
J. Alloy Compounds, 493(1), 438-440 (2010)
A novel high-efficiency visible-light sensitive Ag 2 CO 3 photocatalyst with universal photodegradation performances: Simple synthesis, reaction mechanism and first-principles study.
Dong H, et al.
Applied Catalysis. B, Environmental, 134, 46-54 (2013)
Photocatalytic behavior and photo-corrosion of visible-light-active silver carbonate/titanium dioxide.
Wang Y, et al
Materials Letters, 115, 85-88 (2014)
Sukalyan Bhadra et al.
Journal of the American Chemical Society, 134(24), 9938-9941 (2012-06-12)
Decarboxylative Chan-Evans-Lam-type couplings are presented as a new strategy for the regiospecific construction of diaryl and alkyl aryl ethers starting from easily available aromatic carboxylic acids. They allow converting various aromatic carboxylate salts into the corresponding aryl ethers by reaction
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