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Silver carbonate

Catalog Number
ACM534167
Product Name
Silver carbonate
Structure
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CAS
534-16-7
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Synonyms
Carbonicacid,disilver(1+)salt
IUPAC Name
Disilver;carbonate
Molecular Weight
275.75
Molecular Formula
CAg2O3
Canonical SMILES
C(=O)([O-])[O-].[Ag+].[Ag+]
InChI
InChI=1S/CH₂O3.2Ag/c2-1(3)4;/h(H2,2,3,4);/q;2*+1/p-2
InChI Key
KQTXIZHBFFWWFW-UHFFFAOYSA-L
Melting Point
210 °C
Flash Point
169.8°C
Purity
99%+
Density
6.08 g/mL at 25 °C (lit.)
Solubility
Insoluble in water
Appearance
Green-yellow to greenish granular powder
Storage
Keep in dark place,inert atmosphere,Room Temperature
Assay
0.9999
Complexity
18.8
Covalently-Bonded Unit Count
3
EC Number
208-590-3
Exact Mass
275.79459
H-Bond Acceptor
3
Heavy Atom Count
6
Monoisotopic Mass
273.79493
Odor
Odorless
Stability
Stability Stable, but light sensitive. Incompatible with reducing agents, acids.
Topological Polar Surface Area
63.2 Ų
UNII
V9WU3IKN4Q
Application
Silver carbonate (Ag2CO3) is primarily used as a mild oxidizing agent in organic chemistry, facilitating the conversion of alcohols to aldehydes and ketones. It appears as a light yellow or yellow-green powder, which can darken upon light exposure and decomposes to silver oxide when heated, a process useful for creating other silver compounds. In addition to its role in oxidation reactions, silver carbonate is employed in biological staining and the Koenigs-Knorr glycosylation process. Although not a strong oxidizing agent, it effectively oxidizes alcohols to carbonyl derivatives, as demonstrated by Rapoport's oxidation of codeine to codeinone with a 75% yield, further enhanced in subsequent studies to 85% under varying conditions. Its application extends to the synthesis of complex molecules, such as 3-Oxo-12a-hydroxy-5β-cholanoic Acid, a keto bile acid derivative, using Silver Carbonate on Celite. Despite its limited solubility and reactivity, silver carbonate remains a vital reagent in chemical synthesis due to these versatile applications.
January 27, 2025

Essential Reagent for Organic Synthesis

Silver carbonate proved invaluable in our research laboratory. We used it to oxidize alcohols to aldehydes effectively. Its mild oxidizing properties and high yields make it a reliable choice for organic chemistry experiments.

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