Indolizidine
Appearance
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Names | |
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IUPAC name
Octahydroindolizine
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Other names
δ-Coniceine; 1-Azabicyclo[4.3.0]nonane
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.033.716 |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C8H15N | |
Molar mass | 125.215 g·mol−1 |
Density | 0.8956 g/cm3 (20 °C)[1] |
Boiling point | 159 to 160 °C (318 to 320 °F; 432 to 433 K)[2] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Indolizidine is a heterocyclic chemical compound that forms the central core of the indolizidine alkaloids such as swainsonine and castanospermine.
See also
References
- ^ Skvortsov, I. M.; Zadumina, E. A.; Ponomarev, A. A. (1965). "1-Azabicycles. IV. Catalytic synthesis of 1-azabicyclo[4.3.0]nonanes and 1-azabicyclo[5.3.0]decanes". Khimiya Geterotsiklicheskikh Soedinenii. 6: 864–868.
- ^ Lavagnino, Edward R.; Chauvette, Robert R.; Cannon, William N.; Kornfeld, Edmund C. (1960). "Conidine—Synthesis, Polymerization and Derivatives". Journal of the American Chemical Society. 82 (10): 2609–2613. doi:10.1021/ja01495a054.