Names | |
---|---|
Preferred IUPAC name
Hexahydro-1H-pyrrolizine | |
Other names
Hexahydropyrrolizine 1-Azabicyclo[3.3.0]octane | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider | |
ECHA InfoCard | 100.117.254 |
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C7H13N | |
Molar mass | 111.18 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
Pyrrolizidine is a heterocyclic organic compound that forms the central chemical structure of a variety of alkaloids known collectively as pyrrolizidine alkaloids.[1] It is one of five classes of iminosugars. These are often synthesized from a carbohydrate.[2]
References
- ↑ Pyrrolizidine alkaloids at KEGG Archived 2016-03-03 at the Wayback Machine
- ↑ Lauritsen, Anne; Madsen, Robert (2006-07-19). "Synthesis of naturally occurring iminosugars from D-fructose by the use of a zinc-mediated fragmentation reaction". Organic & Biomolecular Chemistry. 4 (15): 2898–2905. doi:10.1039/B605818C. ISSN 1477-0539. PMID 16855738.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.