Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide

Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide
Names

Other names Methyl-trioctylammonium bis(trifluoromethylsulfonyl)imide
Identifiers
CAS Number	375395-33-8^Y
ChEMBL	ChEMBL561679^N
ChemSpider	17339079^N
Jmol interactive 3D	Image Image
PubChem	16211009
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
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
EU classification (DSD)	Xi
R-phrases	R36/37/38
S-phrases	S26
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).
N verify (what is ^YN ?)
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: 1891–1894. doi:10.1016/s0957-4166(01)00315-9.

This article is issued from Wikipedia - version of the Tuesday, January 26, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.