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Azepane





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Azepane is the organic compound with the formula (CH2)6NH. It is a colorless liquid. A cyclic secondary amine, it is a precursor to several drugs and pesticides. It is produced by partial hydrogenolysisofhexamethylene diamine.[2]

Azepane
Skeletal formula of azepane
Ball-and-stick model of the azepane molecule
Names
Preferred IUPAC name

Azepane

Other names

  • Hexahydroazepine
  • Hexamethyleneimine
  • Homopiperidine
  • Perhydroazepine
  • HMI
  • azacycloheptane

    • Identifiers

    CAS Number

    3D model (JSmol)
    ChEBI
    ChEMBL
    ChemSpider
    ECHA InfoCard 100.003.524 Edit this at Wikidata

    PubChem CID
    UNII

    CompTox Dashboard (EPA)

    • InChI=1S/C6H13N/c1-2-4-6-7-5-3-1/h7H,1-6H2 checkY

      Key: ZSIQJIWKELUFRJ-UHFFFAOYSA-N checkY

    • InChI=1/C6H13N/c1-2-4-6-7-5-3-1/h7H,1-6H2

      Key: ZSIQJIWKELUFRJ-UHFFFAOYAF

    • C1CCCNCC1

    Properties

    Chemical formula

    		 C6H13N
    Molar mass 99.177 g·mol−1
    Appearance colorless liquid
    Density 0.88 g/cm3[1]
    Melting point −37 °C (−35 °F; 236 K)
    Boiling point 138 °C (280 °F; 411 K)[1] (749 mmHg)
    Hazards
    Flash point 30 °C (86 °F; 303 K)

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Like many amines, it reacts with carbon dioxide.[3]

    Azepane-containing drugs

    edit
    1. AK-1 [330461-64-8]
    2. Amicibone
    3. Bazedoxifene
    4. Bacmecillinam (KW 1100)
    5. Brazergoline
    6. BRN 1322519 [4082-37-5][4]
    7. Buzepide (Fenpipramide homolog).
    8. Cetiedil
    9. Gimantan
    10. Glidazamide
    11. Glisoxepide
    12. Glypinamide
    13. Hexacaine
    14. Mecillinam
    15. Molinate
    16. MR-16728 (cetiedil analogue)
    17. Nabazenil
    18. PD-157667
    19. PD-158143
    20. PD-151307
    21. Pincainide
    22. Prozapine
    23. Setastine
    24. Tolazamide
    25. UCL 1608 Fb: [371172-30-4] Oxalate Salt: [371172-31-5]

    See also

    edit

    References

    edit
    1. ^ a b "Hexamethyleneimine".
  • ^ Karsten Eller; Erhard Henkes; Roland Rossbacher; Hartmut Höke (2005). "Amines, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_001. ISBN 3527306730.
  • ^ Sanz-Pérez, E. S.; Arencibia, A.; Sanz, R.; Calleja, G. (2016). "New developments on carbon dioxide capture using amine-impregnated silicas". Adsorption. 22 (4): 366–375. doi:10.1007/s10450-015-9740-2. S2CID 100692983.
  • ^ Barron, D. I.; Hall, G. H.; Natoff, I. L.; Ridley, H. F.; Spickett, R. G. W.; Vallance, D. K. (1965). "Compounds Affecting the Central Nervous System. III. Substituted 1,1-Diaryl-t-aminopropanols and Related Compounds". Journal of Medicinal Chemistry. 8 (6): 836-841. doi:10.1021/jm00330a023.

    • Retrieved from "https://en.wikipedia.org/w/index.php?title=Azepane&oldid=1181484715"
      



    Last edited on 23 October 2023, at 09:32  





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    ●This page was last edited on 23 October 2023, at 09:32 (UTC).
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