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Key Documents

363685

Sigma-Aldrich

Silver carbonate on Celite®

extent of labeling: ~50 wt. % loading

Synonym(s):

Fetizon′s reagent

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About This Item

Linear Formula:
Ag2CO3
CAS Number:
Molecular Weight:
275.75
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23

form

powder and chunks

Quality Level

concentration

45-60 wt. % (by KSCN, titration)

extent of labeling

~50 wt. % loading

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

Application

Employed in the silver ion induced preparation of α-keto acetals and α,α-dialkoxy imines. Catalyzes the generation of stereospecific unsaturated aldehydes from vinylic halides and primary amines.

Legal Information

Celite is a registered trademark of Imerys Minerals California, Inc.

Pictograms

CorrosionEnvironment

Signal Word

Danger

Hazard 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


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Synthesis, 427-427 (1994)
Tetrahedron Letters, 31, 6641-6641 (1990)
Joanna J Buckley et al.
Chemical communications (Cambridge, England), (34)(34), 4013-4015 (2008-09-02)
A simple method of preparing Ag2CO3 nanoparticles utilising high area gamma-alumina nanoneedles has been developed; these are promising antimicrobial agents against diverse bacterial strains.
Yucheng Wang et al.
Biotechnic & histochemistry : official publication of the Biological Stain Commission, 87(5), 346-349 (2012-03-13)
We investigated the character and origin of the newly described "microglia-like" cell in the mammalian organ of Corti after aminoglycoside intoxication. We replicated the neomycin-induced ototoxicity model in cochleae of neonatal Sprague-Dawley rats and used their brains as microglia positive
Congyang Wang et al.
Journal of the American Chemical Society, 131(12), 4194-4195 (2009-03-26)
A novel protocol for the palladium-catalyzed intramolecular direct arylation of benzoic acids is reported, which combines decarboxylation and C-H activation into one efficient process. With the optimized catalyst system of palladium trifluoroacetate, silver carbonate, and the proper solvent mixture (5%

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