Azepine

In this article, we will explore the fascinating world of Azepine. From its origin to its evolution over time, we will delve into its meaning, its importance and its impact on today's society. We will analyze its different facets, from its relevance in the scientific field to its influence on popular culture. Through a multidisciplinary approach, we will highlight the diverse perspectives that exist around Azepine, offering a comprehensive and enriching vision. Thus, we will discover how Azepine has marked a milestone in history and remains a topic of study and debate today.

Azepine
Skeletal formula of azepine
Ball-and-stick model of the Azepine molecule
Names
IUPAC name
Azepine
Other names
Azacycloheptatriene
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C6H7N/c1-2-4-6-7-5-3-1/h1-7H checkY
    Key: XYOVOXDWRFGKEX-UHFFFAOYSA-N checkY
  • InChI=1/C6H7N/c1-2-4-6-7-5-3-1/h1-7H
    Key: XYOVOXDWRFGKEX-UHFFFAOYAM
  • C1=CC=CNC=C1
Properties
C6H7N
Molar mass 93.129 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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Azepines are unsaturated heterocycles of seven atoms, with a nitrogen replacing a carbon at one position.[1][2]

The atoms are numbered starting with the nitrogen. The 1H form shown to the right is unstable and converts to the 3H form.[3]

See also

References

  1. ^ Smith, Jason A.; Molesworth, Peter P.; Hyland, Christopher J. T.; Ryan, John H. (2011-01-01), Gribble, Gordon; Joule, John A. (eds.), Chapter 7 - Seven-Membered Rings, Progress in Heterocyclic Chemistry, vol. 22, Elsevier, pp. 491–536, doi:10.1016/S0959-6380(11)22016-6, ISBN 9780080966854, retrieved 2023-01-05
  2. ^ Császár, Attila G.; Demaison, Jean; Rudolph, Heinz Dieter (2015-03-05). "Equilibrium structures of three-, four-, five-, six-, and seven-membered unsaturated N-containing heterocycles". The Journal of Physical Chemistry A. 119 (9): 1731–1746. Bibcode:2015JPCA..119.1731C. doi:10.1021/jp5084168. ISSN 1520-5215. PMID 25340501.
  3. ^ Römpp Lexikon.
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