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Merck
CN

227277

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
NACRES:
NA.22
PubChem Substance ID:
24853270
UNSPSC Code:
12352100
EC Number:
208-533-2
MDL number:
MFCD00013030

Key Documents

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Product Name

Silver benzoate, 99%

InChI key

CLDWGXZGFUNWKB-UHFFFAOYSA-M

InChI

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

SMILES string

[Ag]OC(=O)c1ccccc1

assay

99%

form

powder or crystals

solubility

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

functional group

phenyl

Quality Level

200

Related Categories

Application

Silver benzoate was used in the synthesis of triphenyltinbenzoate.

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.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS0230
MKCL8211
MKBZ2398V
MKCH3772
MKCC6624

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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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