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363685

Sigma-Aldrich

Silver carbonate on Celite®

extent of labeling: ~50 wt. % loading

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Synonym(s):
Fetizon′s reagent
Linear Formula:
Ag2CO3
CAS Number:
534-16-7
Molecular Weight:
275.75
EC Number:
208-590-3
MDL number:
MFCD00003403
UNSPSC Code:
12352302
PubChem Substance ID:
24862209
NACRES:
NA.23

form

powder and chunks

Quality Level

100

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

Related Categories

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
GHS05,GHS09

Signal Word

Danger

Hazard Statements

H318,H410

Hazard Classifications

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

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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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.
A Ito et al.
The Journal of eukaryotic microbiology, 45(6), 628-636 (1998-12-29)
Morphological features of the rumen ciliate Ostracodinium gracile (Dogiel, 1925) are described from pyridinated silver carbonate-impregnated specimens. Ostracodinium gracile has a characteristic arrangement of infraciliary bands not present in other ophryoscolecid ciliates. Buccal infraciliature is composed of three polybrachykineties. The
Gregory L Hamilton et al.
Journal of the American Chemical Society, 130(45), 14984-14986 (2008-10-22)
Reactions proceeding through cationic intermediates that lack a Lewis or Brønsted basic site present a challenge for traditional asymmetric catalysis based on chiral metals or organocatalysts. We present an enantioselective ring opening of tetrasubstituted meso-aziridinium ions with alcohol nucleophiles proceeding
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