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Contents

   



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1 Formation  




2 Reactions  




3 See also  




4 References  













Oxalyl dicyanide






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From Wikipedia, the free encyclopedia
  

Oxalyl dicyanide
Names
Preferred IUPAC name

Oxalyl dicyanide[1]

Systematic IUPAC name

Ethanedioyl dicyanide

Other names

Oxalyl cyanide
Ethanedioyl cyanide
Dioxosuccinonitrile
2,3-Doxosuccinonitrile
Dioxobutanedinitrile

Identifiers

CAS Number

3D model (JSmol)
ChemSpider

PubChem CID

CompTox Dashboard (EPA)

  • InChI=1S/C4N2O2/c5-1-3(7)4(8)2-6

    Key: VKZZALQGAUWTLQ-UHFFFAOYSA-N

  • N#CC(=O)C(=O)C#N

Properties

Chemical formula

 C4N2O2
Molar mass 108.05 g/mol

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

Oxalyl dicyanide is a chemical compound with the formula C4N2O2.

Formation[edit]

Oxalyl dicyanide can be formed by the hydrolysis of diiminosuccinonitrile.[2]

Reactions[edit]

Oxalyl dicyanide can condense with diaminomaleonitrile to make pyrazinetetracarbonitrile and also 5,6-dihydroxypyrazine-2,3-dicarbonitrile, both derivatives of pyrazine.[2]

See also[edit]

References[edit]

  1. ^ "Front Matter". Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 902. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
  • ^ a b Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 16: Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag. 2014. p. 2035. ISBN 978-3-13-178071-3.
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    • Retrieved from "https://en.wikipedia.org/w/index.php?title=Oxalyl_dicyanide&oldid=978716910"
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