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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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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