Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H5O2.Ag |
| Molecular Weight | 228.9816 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Ag+].[O-]C(=O)C1=CC=CC=C1
InChI
InChIKey=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
| Molecular Formula | Ag |
| Molecular Weight | 107.8682 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C7H5O2 |
| Molecular Weight | 121.1134 |
| Charge | -1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/21112619Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/22674562 | https://www.ncbi.nlm.nih.gov/pubmed/21218074 | http://www.google.com/patents/WO2017067852A1
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21112619
Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/22674562 | https://www.ncbi.nlm.nih.gov/pubmed/21218074 | http://www.google.com/patents/WO2017067852A1
Silver benzoate is a water soluble crystalline salt composed of silver and benzoic acid with the formula C7H5AgO2 with marked antimicrobial activity. Silver benzoate can be used in synthesis of silver nanoparticle, and in the synthesis of triphenyltinbenzoate. 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.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:22:35 GMT 2025
by
admin
on
Mon Mar 31 21:22:35 GMT 2025
|
| Record UNII |
AKL351M7YF
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
CFR |
21 CFR 310.548
Created by
admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
208-533-2
Created by
admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
|
PRIMARY | |||
|
88938
Created by
admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
|
PRIMARY | |||
|
m2363
Created by
admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
|
PRIMARY | Merck Index | ||
|
DTXSID50883426
Created by
admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
|
PRIMARY | |||
|
164649
Created by
admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
|
PRIMARY | |||
|
532-31-0
Created by
admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
|
PRIMARY | |||
|
AKL351M7YF
Created by
admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
|
PRIMARY |