Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide
Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide is an ionic liquid[3] that is produced by Solvent Innovation, now part of EMD Chemicals.
Names | |
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Preferred IUPAC name
N-methyl-N,N-di(octyl)octan-1-aminium bis(trifluoromethanesulfonyl)azanide | |
Other names
Methyl-trioctylammonium bis(trifluoromethylsulfonyl)imide[1] | |
Identifiers | |
3D model (JSmol) |
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ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.157.714 |
EC Number |
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PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C27H54F6N2O4S2 | |
Molar mass | 648.85 g·mol−1 |
Hazards | |
GHS labelling:[2] | |
Warning | |
H315, H319, H335 | |
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P332+P313, P337+P313, P362, P403+P233, P405 | |
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).
Infobox references |
References
- See PubChem
- "Methyltrioctylammonium bis(trifluoromethylsulfonyl)imide". pubchem.ncbi.nlm.nih.gov. Retrieved 12 December 2021.
- 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.
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