CAS 532-31-0 Silver benzoate, 99% - Catalysts / Alfa Chemistry

Synonyms

AC1L4V6M; 114728-EP2292621A1; 114728-EP2298783A1; RTC-061599; UNII-AKL351M7YF; silver benzo-ate; Benzoic acid, silver(1+) salt; MFCD00013030 (95%); silverbenzoate; 532-31-0;

IUPAC Name

silver;benzoate;

Molecular Weight

228.983g/mol

Molecular Formula

C7H5AgO2;

Canonical SMILES

C1=CC=C(C=C1)C(=O)[O-].[Ag+];

InChI

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;

Storage

Store below +30°C.

Complexity

Covalently-Bonded Unit Count

EC Number

208-533-2

Exact Mass

227.934g/mol

H-Bond Acceptor

Heavy Atom Count

Monoisotopic Mass

227.934g/mol

Topological Polar Surface Area

40.1A^2

UNII

AKL351M7YF

Application

Silver benzoate, 99%, is an off-white crystalline powder primarily used as a versatile catalyst in various chemical reactions. It facilitates the conversion of α-amino acids, like D-Alanine, into β-amino acids, such as N-Acetyl-β-alanine. Additionally, silver benzoate serves as an effective catalyst in Wolff rearrangement reactions and, when combined with 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (MTBD), efficiently catalyzes the reaction of carbon dioxide with different ketones. Notably, it also participates in the Hunsdiecker reaction by reacting with bromine in CCl4 to yield C6H5Br. Moreover, silver benzoate plays a role in synthesizing compounds like triphenyltinbenzoate, highlighting its diverse applications in chemical synthesis.

March 10, 2025

Essential Catalyst for Advanced Research Applications

Silver benzoate, 99% from Alfa Chemistry, proved invaluable in synthesizing β-amino acids and facilitating Wolff rearrangement reactions. Its efficiency in CO2-ketone reactions was a game-changer for our lab projects.