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
PubChemCID	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	111.188g·mol−1
	Except where otherwise noted, data are given for materials in theirstandard state(at 25 °C [77 °F], 100 kPa). verify(what is?) Infobox references

Pyrrolizidineis aheterocyclic organic compound.Formally, it is asaturatedderivative ofpyrrolizine.

Pyrrolizidine forms the central chemical structure of a variety ofalkaloidsknown collectively aspyrrolizidine alkaloids.^[1]It is one of five classes ofiminosugars.These are often synthesized from a carbohydrate.^[2]

References

^Pyrrolizidine alkaloidsatKEGG Archived2016-03-03 at theWayback 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 about aheterocyclic compoundis astub.You can help Wikipedia byexpanding it.

[1] Pyrrolizidine alkaloidsatKEGG Archived2016-03-03 at theWayback 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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