Identification | More | [Name]
SILVER BENZOATE | [CAS]
532-31-0 | [Synonyms]
BENZOIC ACID SILVER SALT SILVER BENZOATE SILVER(I) BENZOATE Benzoic acid, silver(1+) salt benzoicacid,silver(1++)salt Silver benzoate (AgOBz) Silver(1+) benzoate Silver benzoate hydrate BENZOIC ACID SILVER Silver(I) benzoate, 98+% AgOBz Benzoic acid silver(I) salt | [EINECS(EC#)]
208-533-2 | [Molecular Formula]
C7H5AgO2 | [MDL Number]
MFCD00013030 | [Molecular Weight]
228.98 | [MOL File]
532-31-0.mol |
Safety Data | Back Directory | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
28432900 |
Hazard Information | Back Directory | [Chemical Properties]
Off-White Crystalline Powder | [Application]
Silver benzoate was used in the synthesis of triphenyltinbenzoate. It is an efficient catalytic system for the reaction of carbon dioxide with various ketones. | [Uses]
Silver benzoate was used in the synthesis of triphenyltinbenzoate. | [Uses]
Silver benzoate is an aromatic salt that is used as a catalyst to prepare β-amino acids (such as N-Acetyl-β-alanine [A168070]) from α-amino acids (such as D-Alanine [A480995]). Silver benzoate is also used as a catalyst in Wolff rearrangement reactions. | [Reactions]
Silver benzoate reacts with bromine in CCl4 refluxing to form C6H5Br This reaction is called Hunsdiecker reaction. | [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. | [Synthesis]
Silver benzoate can be obtained by reacting silver nitrate and sodium benzoate: AgNO3 + PhCOONa → PhCOOAg↓ + NaNO3 Reaction: Mix an equimolar amount of silver nitrate solution with sodium benzoate solution to precipitate silver benzoate. Washed with water and dried in a vacuum desiccator. |
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