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Sigma-Aldrich

Silver benzoate

99%

Synonym(s):

Silver benzoate (AgOBz), Silver(1+) benzoate, Silver(I) benzoate

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About This Item

Linear Formula:
C6H5CO2Ag
CAS Number:
532-31-0
Molecular Weight:
228.98
EC Number:
208-533-2
MDL number:
MFCD00013030
UNSPSC Code:
12352100
PubChem Substance ID:
24853270
NACRES:
NA.22

Quality Level

200

assay

99%

form

powder or crystals

solubility

cold water: 385 part(lit.)
alcohol: slightly soluble(lit.)
hot water: soluble (more soluble)(lit.)

SMILES string

[Ag]OC(=O)c1ccccc1

InChI

1S/C7H6O2.Ag/c8-7(9)6-4-2-1-3-5-6;/h1-5H,(H,8,9);/q;+1/p-1

InChI key

CLDWGXZGFUNWKB-UHFFFAOYSA-M

Related Categories

General description

Silver benzoate along with 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (MTBD) is an efficient catalytic system for the reaction of carbon dioxide with various ketones.

Application

Silver benzoate was used in the synthesis of triphenyltinbenzoate.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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M K Choudhury et al.
Indian journal of pharmaceutical sciences, 72(4), 531-533 (2011-01-11)
Triphenyltinbenzoate was synthesized using triphenyltinchloride and silver benzoate prepared from sodium benzoate. The structure of the synthetic compound was elucidated by spectral and C, H analysis. The antibacterial activities of the organotin compound were determined against four bacteria namely Escherichia
Satoshi Kikuchi et al.
Angewandte Chemie (International ed. in English), 51(28), 6989-6992 (2012-06-08)
A catalytic amount of silver benzoate with 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (MTBD) was an effective catalytic system for the reaction of carbon dioxide with various ketones containing an alkyne group at an appropriate position. These reactions afforded the corresponding γ-lactone derivatives in good

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