Glycidic acid

Glycidic acid
Names
	IUPAC name Oxirane-2-carboxylic acid
Identifiers
CAS Number	503-11-7;
3D model (JSmol)	Interactive image;
ChemSpider	84975;
ECHA InfoCard	100.007.238
PubChem CID	94158;
CompTox Dashboard (EPA)	DTXSID70964569 ;
	InChI InChI=1S/C3H4O3/c4-3(5)2-1-6-2/h2H,1H2,(H,4,5) Key: OTGHWLKHGCENJV-UHFFFAOYSA-N; InChI=1/C3H4O3/c4-3(5)2-1-6-2/h2H,1H2,(H,4,5) Key: OTGHWLKHGCENJV-UHFFFAOYAU;
	SMILES C1C(O1)C(=O)O;
Properties
Chemical formula	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).
	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.

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): 7549–59. doi:10.1002/chem.201101001. PMID 21647994.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.