Indolizidine
From Wikipedia, the free encyclopedia
Indolizidine | |
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IUPAC name Octahydroindolizine | |
Other names δ-Coniceine; 1-Azabicyclo[4.3.0]nonane | |
Identifiers | |
CAS number | 13618-93-4 |
PubChem | 26136 |
ChemSpider | 24347 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C8H15N |
Molar mass | 125.21 g mol−1 |
Density | 0.8956 g/cm3 (20 °C)[1] |
Boiling point | 159-160 °C[2] |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
Infobox references | |
Indolizidine is a heterocyclic chemical compound that forms the central core of the indolizidine alkaloids such as swainsonine.
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.
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