Pyrrolizidine

Pyrrolizidine
Names
	Preferred IUPAC name Hexahydro-1H-pyrrolizine
	Other names Hexahydropyrrolizine; 1-Azabicyclo[3.3.0]octane
Identifiers
CAS Number	643-20-9 ;
3D model (JSmol)	Interactive image;
ChemSpider	12039 ;
ECHA InfoCard	100.117.254
PubChem CID	12558;
UNII	U81KWZ2JKN ;
CompTox Dashboard (EPA)	DTXSID00214524 ;
	InChI InChI=1S/C7H13N/c1-3-7-4-2-6-8(7)5-1/h7H,1-6H2 Key: ADRDEXBBJTUCND-UHFFFAOYSA-N ; InChI=1/C7H13N/c1-3-7-4-2-6-8(7)5-1/h7H,1-6H2 Key: ADRDEXBBJTUCND-UHFFFAOYAT;
	SMILES N12CCCC1CCC2;
Properties
Chemical formula	C7H13N
Molar mass	111.188 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Pyrrolizidine is a heterocyclic organic compound. Formally, it is a saturated derivative of pyrrolizine.

Pyrrolizidine 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.

[1] Pyrrolizidine alkaloids at KEGG Archived 2016-03-03 at the Wayback Machine

[2] 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.

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