Date published: 2025-12-10

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Silver benzoate (CAS 532-31-0)

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Alternate Names:
Silver benzoate (AgOBz); Silver(1+) benzoate; Silver(I) benzoate
Application:
Silver benzoate is an efficient catalytic system for the reaction of carbon dioxide with various ketones
CAS Number:
532-31-0
Molecular Weight:
228.98
Molecular Formula:
C7H5AgO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Silver benzoate was used in the synthesis of triphenyltinbenzoate. It is an efficient catalytic system for the reaction of carbon dioxide with various ketones. Silver benzoate is also used as a catalyst in Wolff rearrangement reactions. It is a white powder that is soluble in organic solvents such as ethanol and acetone but insoluble in water.


Silver benzoate (CAS 532-31-0) References

  1. Single phase preparation of monodispersed silver nanoclusters using a unique electron transfer and cluster stabilising agent, triethylamine.  |  Chaki, NK., et al. 2002. Chem Commun (Camb). 76-7. PMID: 12120318
  2. Biochemical studies of toxic agents. 13. The metabolism of acenaphthylene.  |  HOPKINS, RP., et al. 1962. Biochem J. 82: 457-66. PMID: 14448806
  3. Silver-nanoparticle-embedded antimicrobial paints based on vegetable oil.  |  Kumar, A., et al. 2008. Nat Mater. 7: 236-41. PMID: 18204453
  4. Synthesis and antibacterial activity of triphenyltinbenzoate.  |  Choudhury, MK. and Zewdie, B. 2010. Indian J Pharm Sci. 72: 531-3. PMID: 21218074
  5. C-C bond formation with carbon dioxide promoted by a silver catalyst.  |  Kikuchi, S., et al. 2012. Angew Chem Int Ed Engl. 51: 6989-92. PMID: 22674562
  6. Effect of silver-loaded PMMA on Streptococcus mutans in a drip flow reactor.  |  Williams, DL., et al. 2017. J Biomed Mater Res A. 105: 2632-2639. PMID: 28512783
  7. A Predictive Model for the Decarboxylation of Silver Benzoate Complexes Relevant to Decarboxylative Coupling Reactions.  |  Crovak, RA. and Hoover, JM. 2018. J Am Chem Soc. 140: 2434-2437. PMID: 29381354
  8. Silver Benzoate Facilitates the Copper-Catalyzed C-N Coupling of Iodoazoles with Aromatic Nitrogen Heterocycles.  |  Lozano, C., et al. 2021. ACS Omega. 6: 9804-9812. PMID: 33869960
  9. K2S2O8-Mediated Synthesis of Highly Functionalized Pyrroles via Oxidative Self-Dimerization of N-Propargylamines.  |  Behera, BK., et al. 2021. J Org Chem. 86: 12481-12493. PMID: 34463507
  10. Synthesis and beta-lactamase inhibitory properties of 2 beta-[(acyloxy)methyl]-2-methylpenam-3 alpha-carboxylic acid 1,1-dioxides.  |  Gottstein, WJ., et al. 1985. J Med Chem. 28: 518-22. PMID: 3872369
  11. Properties of silver sulfadiazine-resistant Enterobacter cloacae.  |  Rosenkranz, HS., et al. 1974. Antimicrob Agents Chemother. 5: 199-201. PMID: 4840432
  12. Hydroxy-steroids. VI. Reactions of olefins with silver salts and iodine.  |  Ellington, PS., et al. 1966. J Chem Soc Perkin 1. 15: 1327-31. PMID: 5949484
  13. A facile synthesis of 5 beta-cholestane-3 alpha,7 alpha,12 alpha,25-tetrol.  |  Dayal, B., et al. 1980. Steroids. 35: 439-44. PMID: 7376230

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Silver benzoate, 10 g

sc-236878
10 g
$63.00