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.
Names | |
---|---|
Preferred IUPAC name
Oxiranecarboxylic acid | |
Identifiers | |
3D model (JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.007.238 |
PubChem CID
|
|
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C3H4O3 | |
Molar mass | 88.062 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
See also
editReferences
edit- ^ 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): 7549–59. doi:10.1002/chem.201101001. PMID 21647994.