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Azocine

From Wikipedia, the free encyclopedia
Azocine
Names
Preferred IUPAC name
(3Z,5Z,7Z)-Azocine
Other names
Azacyclooctatetraene
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C7H7N/c1-2-4-6-8-7-5-3-1/h1-7H/b2-1-,3-1-,4-2-,5-3-,6-4-,7-5-,8-6-,8-7- checkY
    Key: XXRGLCKZBCIEKO-BONZMOEMSA-N checkY
  • InChI=1/C7H7N/c1-2-4-6-8-7-5-3-1/h1-7H/b2-1-,3-1-,4-2-,5-3-,6-4-,7-5-,8-6-,8-7-
    Key: XXRGLCKZBCIEKO-BONZMOEMBP
  • N=1\C=C/C=C\C=C/C=1
Properties
C7H7N
Molar mass 105.140 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkYX markN ?)

Azocine is a heterocyclic organic compound with the molecular formula C7H7N. It consists of an unsaturated eight-membered ring having seven carbon atoms, one nitrogen atom and four double bonds.

The parent compound is thermally unstable and polymerizes at −50 °C. It can be prepared temporarily through diazabasketene pyrolysis: a retro-Diels–Alder decomposition and subsequent hydrocyanic acid elimination.[1]

Nakadomarin A

Nevertheless, azocine-type rings are found in many natural products. The potential antibiotic nakadomarin A, a manzamine-type marine alkaloid, contains a partially saturated azocine within its fused, hexacyclic ring system.

Saturated or partially saturated azocine rings also form the core structure defining the azocine opioid family. These include cyclazocine, pentazocine, and phenazocine.

See also

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References

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  1. ↑ Theophil Eicher, Siegfried Hauptmann, Andreas Speicher (2012), The Chemistry of Heterocycles. Wiley-VCH, ISBN 978-3-527-32747-8. pp. 547–549.
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