Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide

Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide
Names
	Other names Methyl-trioctylammonium bis(trifluoromethylsulfonyl)imide[citation needed]
Identifiers
CAS Number	375395-33-8 ;
3D model (JSmol)	Interactive image; Interactive image;
ChEMBL	ChEMBL561679 ;
ChemSpider	17339079 ;
ECHA InfoCard	100.157.714
PubChem CID	16211009;
UNII	939A0J7H68 ;
CompTox Dashboard (EPA)	DTXSID3047926 ;
	InChI InChI=1S/C25H54N.C2F6NO4S2/c1-5-8-11-14-17-20-23-26(4,24-21-18-15-12-9-6-2)25-22-19-16-13-10-7-3;3-1(4,5)14(10,11)9-15(12,13)2(6,7)8/h5-25H2,1-4H3;/q+1;-1 Key: LAGQNGWYNLUQRI-UHFFFAOYSA-N ;
	SMILES FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F.CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC; O=S([N-]S(=O)(C(F)(F)F)=O)(C(F)(F)F)=O.CCCCCCCC[N+](CCCCCCCC)(C)CCCCCCCC;
Properties
Chemical formula	C27H54F6N2O4S2
Molar mass	648.85 g·mol−1
Hazards
Flash point	>110 °C
Related compounds
Related compounds	Bistriflimide
	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

Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide is an ionic liquid^[1] that is produced by Solvent Innovation, now part of EMD Chemicals.

References

^ Fraile, J. M.; Garcia, J. I.; Herrerias, C. I.; Mayoral, J. A.; Carrie, D.; Vaultier, M. (2001). "Enantioselective cyclopropanation reactions in ionic liquids". Tetrahedron: Asymmetry. 12 (13): 1891–1894. doi:10.1016/s0957-4166(01)00315-9. hdl:10261/64635.

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

[1] Fraile, J. M.; Garcia, J. I.; Herrerias, C. I.; Mayoral, J. A.; Carrie, D.; Vaultier, M. (2001). "Enantioselective cyclopropanation reactions in ionic liquids". Tetrahedron: Asymmetry. 12 (13): 1891–1894. doi:10.1016/s0957-4166(01)00315-9. hdl:10261/64635.

[1]