Chemistry:Indolizidine
From HandWiki
Names | |
---|---|
IUPAC name
Octahydroindolizine
| |
Other names
δ-Coniceine; 1-Azabicyclo[4.3.0]nonane
| |
Identifiers | |
3D model (JSmol)
|
|
ChemSpider | |
PubChem CID
|
|
UNII | |
| |
| |
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). | |
Infobox references | |
Tracking categories (test):
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.
Original source: https://en.wikipedia.org/wiki/Indolizidine.
Read more |