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Merck
CN

920991

Silver(I) carbonate

≥99.9% trace metals basis

Synonym(s):

Silver carbonate

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About This Item

Linear Formula:
Ag2CO3
CAS Number:
Molecular Weight:
275.75
NACRES:
NA.23
UNSPSC Code:
12352302
Beilstein/REAXYS Number:
6936654
MDL number:
Assay:
≥99.9% trace metals basis
Form:
powder
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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

assay

≥99.9% trace metals basis

form

powder

reaction suitability

core: silver

mp

210 °C (dec.) (lit.)

density

6.08 g/mL at 25 °C (lit.)

application(s)

PEM fuel cells
material synthesis precursor

Quality Level

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Application

Silver carbonate can be used as a catalyst to synthesize α-trifluoromethylacrylic acids and 2-(pyridin-3-yl)pyrimidines (PPMDs), key building blocks for synthesizing bioactive molecules. Additionally, Ag2CO3 can also be used to functionalize metallofullerenes with potential photovoltaic and biomedical applications.

pictograms

CorrosionEnvironment

signalword

Danger

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

Storage Class

13 - Non Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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Ligand Free Palladium-Catalyzed Synthesis of a-Trifluoromethylacrylic Acids and Related Acrylates by Three-Component Reaction
Xiao P, et al.
Advanced Synthesis & Catalysis, 362(4), 949-954 (2020)
Silver-catalyzed cascade reactions of 3-cyanochromone with 1, 1-enediamines: synthesis of highly functionalized 2-(pyridin-3-yl)-chromeno [2, 3-d] pyrimidines.
Xiao Q, et al.
Organic Chemistry Frontiers : An International Journal of Organic Chemistry / Royal Society of Chemistry, 7(15), 2035-2039 (2020)
Jia Li et al.
Frontiers in chemistry, 8, 593602-593602 (2020-11-17)
A novel radical reaction of monometallofullerene Y@C2v(9)-C82 with N-arylbezamidine (1) is successfully conducted through catalysis with silver carbonate. The high-performance liquid chromatographic and mass spectrum results demonstrate that the reaction is highly regioselective to afford only one monoadduct (2) with

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