Nitroamine
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In organic and inorganic chemistry, nitroamines or nitramides are chemical compounds with the general chemical structure Page Module:Chem2/styles.css has no content.R1R2N−NO2. They consist of a nitro group (Page Module:Chem2/styles.css has no content.−NO2) bonded to the nitrogen of an amine.[1][2] The R groups can be any group, typically hydrogen (e.g., methylnitroamine Page Module:Chem2/styles.css has no content.CH3−NH−NO2) and organyl (e.g., diethylnitroamine Page Module:Chem2/styles.css has no content.(CH3CH2−)2N−NO2). An example of inorganic nitroamine is chloronitroamine, Page Module:Chem2/styles.css has no content.Cl−NH−NO2.[3] The parent inorganic compound, where both R substituents are hydrogen, is nitramide or nitroamine, Page Module:Chem2/styles.css has no content.H2N−NO2.
N-Nitroaniline rearranges in the presence of acid to give 2-nitroaniline.[4]
References
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- ^ Page Module:Citation/CS1/styles.css has no content.Clayden, J.; Greeves, N.; Warren, S.; Wothers, P. (2001). Organic Chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.
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- ^ Page Module:Citation/CS1/styles.css has no content."N-chloronitramide".
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Further reading
- Page Module:Citation/CS1/styles.css has no content.Schmidt, Eckart W. (2022). "Nitramines". Encyclopedia of Liquid Fuels. De Gruyter. pp. 4203–4413. doi:10.1515/9783110750287-035. ISBN 978-3-11-075028-7.
