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Silver benzoate, 99%

Catalog Number
ACM532310-1
Product Name
Silver benzoate, 99%
Structure
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CAS
532-31-0
  • Product Overview
  • Usage
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
98
Covalently-Bonded Unit Count
2
EC Number
208-533-2
Exact Mass
227.934g/mol
H-Bond Acceptor
2
Heavy Atom Count
10
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.
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