Organic isocyanides
Organic isocyanides are a class of chemical compounds containing the functional group -N=C=O, where carbon is bonded to both an alkyl or aryl group and an isocyanate group. These reactive intermediates play a crucial role in various synthetic chemistry applications due to their ability to undergo addition reactions with a wide range of nucleophiles.
Isocyanides are often used as precursors in the synthesis of amides, ureas, and other functionalized organic molecules. They can be derived from isocyanates through reduction processes or obtained directly via the Grignard reaction. Due to their reactivity, they require careful handling under protective atmospheres such as nitrogen to prevent unwanted side reactions.
In addition to their synthetic utility, some isocyanides are also used in industries like pharmaceuticals and agrochemicals for the production of bioactive compounds. Their unique properties make them valuable tools in organic synthesis and materials science research.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Tert-BUTYL ISOCYANIDE | 7188-38-7 | C5H9N |
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Isocyanomethane | 593-75-9 | C2H3N |
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Cyclohexene, 1-(2-isocyanoethyl)- | 172223-58-4 | C9H13N |
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Cyclohexane,1,4-diisocyano- | 935-15-9 | C8H10N2 |
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7-Isocyano-14-isocycloamphilectene | 175861-81-1 | C21H31N |
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Mirabilene D isonitrile | 128052-85-7 | C24H39NO4 |
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Mirabilene E isonitrile | 127999-49-9 | C24H39NO4 |
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Mirabilene A isonitrile | 127999-47-7 | C24H41NO4 |
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Isocyanoallopupukeanane | 138949-83-4 | C16H25N |
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7-Isocyano-11-cycloamphilectene | 108695-80-3 | C21H31N |
Related Literature
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
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Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
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Abdelaziz Houmam,Emad M. Hamed Chem. Commun., 2012,48, 11328-11330
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Bo Wei,Zhenyu Liu,Chen Xie,Shu Yang,Wentao Tang,Aiwei Gu,Wing-Tak Wong,Ka-Leung Wong J. Mater. Chem. C, 2015,3, 12322-12327
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
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