氧代丙二腈

氧代丙二腈
別名	碳醯腈; 羰基氰化物
識別
CAS號	1115-12-4
SMILES	N#CC(=O)C#N;
性質
化學式	C3N2O
摩爾質量	80.04 g·mol−1
溶解性（水）	可溶於乙醚
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

氧代丙二腈是一種有機化合物，化學式為C₃N₂O。它可由四氰基環氧乙烷和甲硫醚反應製得。^[1]它可以和六氟銻酸銀在二氧化硫中於低溫反應，得到含陽離子框架的[Ag{NCC(O)CN}₂]_n[SbF₆]_n。^[2]它和乙烯酮反應，可以得到β,β-二氰基丙內酯。^[3]它可用於氰甲酸酯的合成。^[1]

參考文獻

^ ^1.0 ^1.1 Rondla, Naveen R.; Levi, Samuel M.; Ryss, Jonathan M.; Vanden Berg, Rachel A.; Douglas, Christopher J. Palladium-Catalyzed C−CN Activation for Intramolecular Cyanoesterification of Alkynes. Organic Letters (American Chemical Society (ACS)). 2011-03-21, 13 (8): 1940–1943. ISSN 1523-7060. doi:10.1021/ol200274h.
^ Decken, Andreas; Knapp, Carsten; Passmore, Jack. [Ag{NCC(O)CN}2]n [SbF6]n, the first metal complex of carbonyl cyanide. Journal of Chemical Crystallography (Springer Science and Business Media LLC). 2005, 35 (9): 697–700. ISSN 1074-1542. doi:10.1007/s10870-005-3618-1.
^ Hyatt, John A.; Raynolds, Peter W., Ketene Cycloadditions, Wiley, 1994-06-10, ISBN 978-0-471-26418-7, doi:10.1002/0471264180.or045.02

[Rondla-1] 1.0 ^1.1 Rondla, Naveen R.; Levi, Samuel M.; Ryss, Jonathan M.; Vanden Berg, Rachel A.; Douglas, Christopher J. Palladium-Catalyzed C−CN Activation for Intramolecular Cyanoesterification of Alkynes. Organic Letters (American Chemical Society (ACS)). 2011-03-21, 13 (8): 1940–1943. ISSN 1523-7060. doi:10.1021/ol200274h.

[2] Decken, Andreas; Knapp, Carsten; Passmore, Jack. [Ag{NCC(O)CN}2]n [SbF6]n, the first metal complex of carbonyl cyanide. Journal of Chemical Crystallography (Springer Science and Business Media LLC). 2005, 35 (9): 697–700. ISSN 1074-1542. doi:10.1007/s10870-005-3618-1.

[3] Hyatt, John A.; Raynolds, Peter W., Ketene Cycloadditions, Wiley, 1994-06-10, ISBN 978-0-471-26418-7, doi:10.1002/0471264180.or045.02

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