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Contents

   



(Top)
  


1 See also  




2 References  













Glycidic acid






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From Wikipedia, the free encyclopedia
  

Glycidic acid
Names
Preferred IUPAC name

Oxiranecarboxylic acid

Identifiers

CAS Number

3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.238 Edit this at Wikidata

PubChem CID

CompTox Dashboard (EPA)

  • 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

  • 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.

See also

[edit]

References

[edit]
  1. ^ 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.

    • Retrieved from "https://en.wikipedia.org/w/index.php?title=Glycidic_acid&oldid=1184286818"
    Categories: 
    ●Carboxylic acids
     ●Epoxides
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