Advertisement

Chemistry of Heterocyclic Compounds

, Volume 28, Issue 3, pp 309–313 | Cite as

Synthesis and structure of 6-hydrazino-2,4,5-trichloronicotinonitrile

  • V. G. Kvartsev
  • É. M. Gizatullina
  • Z. G. Aliev
Article
  • 25 Downloads

Abstract

The reaction of tetrachloronicotinonitrile with hydrazine hydrate has been studied. The structure of the reaction product has been established based on x-ray structural analysis.

Keywords

Hydrate Organic Chemistry Structural Analysis Hydrazine Hydrazine Hydrate 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    H. Suschitzky, I. Collins, and S. M. Robert, J. Chem. Soc., C, No. 1, 167 (1971).Google Scholar
  2. 2.
    S. M. Robert and H. Suschitzky, Chem. Commun., No. 17, 893 (1967).Google Scholar
  3. 3.
    A. Roedig, K. Grohe, and D. Klatt, Ber., 99, 2818 (1966).Google Scholar
  4. 4.
    A. Roedig and K. Grohe, Ber., 98, 923 (1965).Google Scholar
  5. 5.
    M. Lacan and T. Tabakovic, Croat. Chem. Acta, 47, 127 (1975).Google Scholar
  6. 6.
    L. Kuczynski, A. Mrozikiewics, W. Banaszkiewics, and K. Poreba, Pol. J. Pharmacol. Pharm., 31, 217 (1979).Google Scholar
  7. 7.
    Ger. Offen. (Patent) 2643753; J. Roch, E. Mueller, B. Narr, J. Nickl, and W. Haarmann, Chem. Abstracts, 89, 6322r (1978).Google Scholar
  8. 8.
    A. I. Kitaigorodskii, P. M. Zorkii, and V. K. Bel'skii, Structure of Organic Compounds [in Russian], Nauka, Moscow (1980).Google Scholar
  9. 9.
    E. Bayer and G. Hafelinger, Ber., 99, 1689 (1966).Google Scholar
  10. 10.
    M. Laing, N. Sparrow, and P. Sommerville, Acta Cryst. Sect. B, 27, 1986 (1971).Google Scholar
  11. 11.
    A. Aasen, E. G. Iversen, and B. Klewe, Acta Chem. Scand., Ser. A, 29, 381 (1975).Google Scholar
  12. 12.
    N. W. Alcock and C. J. Samuel, J. Chem. Soc., Chem. Commun., No. 11, 603 (1982).Google Scholar
  13. 13.
    J. C. Daran, G. Jennin, and L. M. Martin, Acta Cryst. Sect. B, 35, 3030 (1979).Google Scholar
  14. 14.
    U. S. Patent No. 4087431; S. D. McGregor, Chem. Abstracts, 89, 109124g (1978).Google Scholar
  15. 15.
    U. S. Patent No. 3325503; R. M. Bimber, Chem. Abstracts, 68, 68896f (1968).Google Scholar

Copyright information

© Plenum Publishing Corporation 1992

Authors and Affiliations

  • V. G. Kvartsev
    • 1
  • É. M. Gizatullina
    • 1
  • Z. G. Aliev
    • 1
  1. 1.Institute of Chemical PhysicsRussian Academy of SciencesChernogolovka

Personalised recommendations