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| Names | |
|---|---|
|
Preferred IUPAC name
Oxalyl dicyanide
[1] | |
|
Systematic IUPAC name
Ethanedioyl dicyanide | |
| Other names
Oxalyl cyanide
Ethanedioyl cyanide Dioxosuccinonitrile 2,3-Doxosuccinonitrile Dioxobutanedinitrile | |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| 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).
| |
Oxalyl dicyanide is a chemical compound with the formula C4 N2 O2.
Oxalyl dicyanide can be formed by the hydrolysis of diiminosuccinonitrile. [2]
Oxalyl dicyanide can condense with diaminomaleonitrile to make pyrazinetetracarbonitrile and also 5,6-dihydroxypyrazine-2,3-dicarbonitrile, both derivatives of pyrazine. [2]
- ^ "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.
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
|
| |
| Names | |
|---|---|
|
Preferred IUPAC name
Oxalyl dicyanide
[1] | |
|
Systematic IUPAC name
Ethanedioyl dicyanide | |
| Other names
Oxalyl cyanide
Ethanedioyl cyanide Dioxosuccinonitrile 2,3-Doxosuccinonitrile Dioxobutanedinitrile | |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| 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).
| |
Oxalyl dicyanide is a chemical compound with the formula C4 N2 O2.
Oxalyl dicyanide can be formed by the hydrolysis of diiminosuccinonitrile. [2]
Oxalyl dicyanide can condense with diaminomaleonitrile to make pyrazinetetracarbonitrile and also 5,6-dihydroxypyrazine-2,3-dicarbonitrile, both derivatives of pyrazine. [2]
- ^ "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.
|
| This article about an organic compound is a stub. You can help Wikipedia by expanding it. |