Monomorine I

Monomorine I
Names
	Preferred IUPAC name (3R,5S,8aS)-3-Butyl-5-methyloctahydroindolizine
	Other names 5-Methyl-3-butyloctahydroindolizine
Identifiers
CAS Number	53447-44-2 ;
3D model (JSmol)	Interactive image;
ChemSpider	161465;
PubChem CID	185741;
UNII	8EBV7G2L35 ;
CompTox Dashboard (EPA)	DTXSID50968121 ;
	InChI InChI=1S/C13H25N/c1-3-4-7-12-9-10-13-8-5-6-11(2)14(12)13/h11-13H,3-10H2,1-2H3/t11-,12+,13-/m0/s1 Key: HFUFMWLNHRIKMV-XQQFMLRXSA-N; InChI=1/C13H25N/c1-3-4-7-12-9-10-13-8-5-6-11(2)14(12)13/h11-13H,3-10H2,1-2H3/t11-,12+,13-/m0/s1 Key: HFUFMWLNHRIKMV-XQQFMLRXBR;
	SMILES CCCC[C@@H]1CC[C@H]2N1[C@H](CCC2)C;
Properties
Chemical formula	C13H25N
Molar mass	195.350 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Monomorine I is a bicyclic amine that is the trail pheromone of Monomorium pharaonis. Its structure was first elucidated 1973.^[1] Synthetic monomorine might be used to lure ants to their doom.^[2]

References

↑ Ritter, F. J.; Rotgans, I. E. M.; Talman, E.; Verwiel, P. E. J.; Stein, F. (1 May 1973). "5-methyl-3-butyl-octahydroindolizine, a novel type of pheromone attractive to Pharaoh's ants (Monomorium pharaonis (L.)". Experientia. 29 (5): 530–531. doi:10.1007/BF01926645. S2CID 37818885.
↑ Wyatt, Stuart Warren, Paul (2008). Organic synthesis : the disconnection approach (2nd ed.). Oxford: Wiley-Blackwell. ISBN 978-0470712368.{{cite book}}: CS1 maint: multiple names: authors list (link)

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[1] Ritter, F. J.; Rotgans, I. E. M.; Talman, E.; Verwiel, P. E. J.; Stein, F. (1 May 1973). "5-methyl-3-butyl-octahydroindolizine, a novel type of pheromone attractive to Pharaoh's ants (Monomorium pharaonis (L.)". Experientia. 29 (5): 530–531. doi:10.1007/BF01926645. S2CID 37818885.

[2] Wyatt, Stuart Warren, Paul (2008). Organic synthesis : the disconnection approach (2nd ed.). Oxford: Wiley-Blackwell. ISBN 978-0470712368.{{cite book}}: CS1 maint: multiple names: authors list (link)

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References