Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide

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Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide

Other names Methyl-trioctylammonium bis(trifluoromethylsulfonyl)imide^{[citation needed]}
Identifiers
CAS number	375395-33-8^Y
PubChem	16211009
ChemSpider	17339079^N
ChEMBL	CHEMBL561679^N
Jmol-3D images	{{#if:O=S([N-]S(=O)(C(F)(F)F)=O)(C(F)(F)F)=O.CCCCCCCC[N+](CCCCCCCC)(C)CCCCCCCC\|Image 1
SMILES O=S([N-]S(=O)(C(F)(F)F)=O)(C(F)(F)F)=O.CCCCCCCC[N+](CCCCCCCC)(C)CCCCCCCC
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^N Key: LAGQNGWYNLUQRI-UHFFFAOYSA-N^N
Properties
Molecular formula	C₂₇H₅₄F₆N₂O₄S₂
Molar mass	648.85 g mol⁻¹
Hazards
EU classification	Xi
R-phrases	R36/37/38
S-phrases	S26
Flash point	>110 °C
Related compounds
Related compounds	Bistriflimide
N (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
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.

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