Glycidic acid
 | |
| Names | |
|---|---|
| IUPAC name
2-Oxiranecarboxylic acid | |
| Identifiers | |
| 503-11-7 | |
| 3D model (Jmol) | Interactive image |
| ChemSpider | 84975 |
| ECHA InfoCard | 100.007.238 |
| PubChem | 94158 |
| |
| |
| Properties | |
| C3H4O3 | |
| Molar mass | 88.06 g·mol−1 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Glycidic acid is an organic compound that has both epoxide and carboxylic acid functions. It may be prepared by the oxidation of glycidol,[1] or by the epoxidation of acrylic acid.[2] This compound is commercially available as well.
See also
References
- ↑ More, Swati S.; Vince, Robert (2008). "Design, Synthesis and Biological Evaluation of Glutathione Peptidomimetics as Components of Anti-Parkinson Prodrugs". Journal of Medicinal Chemistry. 51 (15): 4581–8. doi:10.1021/jm800239v. PMID 18651729.
- ↑ Kamata, Keigo; Sugahara, Kosei; Yonehara, Kazuhiro; Ishimoto, Ryo; Mizuno, Noritaka (2011). "Efficient Epoxidation of Electron-Deficient Alkenes with Hydrogen Peroxide Catalyzed by \γ-PW10O38V2(μ-OH)2]3−". Chemistry: A European Journal. 17 (27): 7549. doi:10.1002/chem.201101001.
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