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imenes imidic acids

imides

  1. Diacyl derivatives of ammonia or primary amines, especially those cyclic compounds derived from diacids, e.g.
    I02948
  2. In additive nomenclature, in which imide is analogous to oxide, the term is used to name compounds of the type R3Y+–N−R (Y = N, P) and R2Z+–N−R (Z = O, S, Se, Te), which are the products of formal attachment of an RN= group to N, P, O, S, Se, Te. E.g. amine imides, azomethine imides.
  3. Salts having the anionRN2−.
Source:
PAC, 1995, 67, 1307 (Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995)) on page 1342
InChI=1/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7)/f/h5H
InChI=1/C3H5NO3S/c5-3-1-2-8(6,7)4-3/h1-2H2,(H,4,5)/f/h4H
KZNICNPSHKQLFF-JSWHHWTPCC
ASJJYLPJOJGZAW-JLSKMEETCJ
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IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. https://doi.org/10.1351/goldbook.
Last update: 2014-02-24; version: 2.3.3.
DOI of this term: https://doi.org/10.1351/goldbook.I02948.
Original PDF version: http://www.iupac.org/goldbook/I02948.pdf. The PDF version is out of date and is provided for reference purposes only. For some entries, the PDF version may be unavailable.
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