Silver salicylate
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| Surname | Silver salicylate | |||||||||
| Molecular formula | C 7 H 5 AgO 3 | |||||||||
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| Molar mass | 244.99 g mol −1 | |||||||||
| Physical state |
firmly |
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| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . | ||||||||||
Silver salicylate is a chemical compound of silver from the group of salicylates .
Extraction and presentation
Silver salicylate can be obtained by reacting a solution of salicylic acid in ethanol with silver nitrate at 60-70 ° C.
properties
Silver salicylate is a white solid which, as a hydrate, is sparingly soluble in water.
use
Silver salicylate can be used as an intermediate in the manufacture of drugs. It also serves as a catalyst for the classic Koenigs-Knorr reaction , as an accelerator for the heavy metal-assisted cleavage of thiazolidine rings and in the nucleophilic displacement of alkyl iodides .
Individual evidence
- ↑ a b c d e f Nycholat, CM and Lowary, TL: Silver Salicylate . In: e-EROS Encyclopedia of Reagents for Organic Synthesis . 2005, doi : 10.1002 / 047084289X.rn00545 .
- ↑ a b c d e f g Data sheet Silver salicylate hydrate from AlfaAesar, accessed on March 17, 2018 ( PDF )(JavaScript required) .
- ↑ Franz v. Bruchhausen, Siegfried Ebel, Eberhard Hackenthal, Ulrike Holzgrabe: Hager's Handbook of Pharmaceutical Practice, Volume 5: Substances LZ . Springer-Verlag, 2013, ISBN 978-3-642-58388-9 , pp. 222 ( limited preview in Google Book search).