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Merck
모든 사진(1)

주요 문서

727725

Sigma-Aldrich

1-Butyl-1-methylpyrrolidinium trifluoromethanesulfonate

95%

동의어(들):

BMPyrrOTf

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About This Item

실험식(Hill 표기법):
C10H20F3NO3S
CAS Number:
Molecular Weight:
291.33
Beilstein:
9820503
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

≥95.0% (T)
95%

형태

liquid

불순물

≤0.3% water

작용기

fluoro
triflate

SMILES string

[O-]S(=O)(=O)C(F)(F)F.CCCC[N+]1(C)CCCC1

InChI

1S/C9H20N.CHF3O3S/c1-3-4-7-10(2)8-5-6-9-10;2-1(3,4)8(5,6)7/h3-9H2,1-2H3;(H,5,6,7)/q+1;/p-1

InChI key

WZJDNKTZWIOOJE-UHFFFAOYSA-M

애플리케이션

1-Butyl-1-methylpyrrolidinium trifluoromethanesulfonate ([BMPy][OTf]) is an ionic liquid that can be used as a solvent in:
  • Rhodium-catalyzed regioselective hydroformylation reactions.
  • Direct asymmetric aldol condensation reaction.
  • Desulfurization of fuels.
  • Nucleophilic aromatic substitution reactions.

([BMPy][OTf]) can also be used as an electrolyte in supercapacitor applications.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리 방문

An improved protocol for the direct asymmetric aldol reaction in ionic liquids, catalysed by onium ion-tagged prolines
Lombardo M, et al.
Advanced Synthesis & Catalysis, 349(11-12), 2061-2065 (2007)
Effect of the cation and anion of the ionic liquid on desulfurization of model fuels
Domanska U and Wlazlo M
Fuel: The Science and Technology of Fuel and Energy, 134(11-12), 114-125 (2014)
Andrzej Lewandowski et al.
Journal of solution chemistry, 42(2), 251-262 (2013-03-14)
The electrochemical behavior of cobaltocenium has been studied in a number of room temperature aprotic ionic liquids. Well defined, diffusion controlled, anodic and cathodic peaks were found for the Cc
An improved protocol for the direct asymmetric aldol reaction in ionic liquids, catalysed by onium ion-tagged prolines
Lombardo M, et al.
advanced synthesis and catalysis, 349(11-12), 2061-2065 (2007)
Ionic liquids as designer solvents for nucleophilic aromatic substitutions
Newington I, et al.
Organic Letters, 9(25), 5247-5250 (2007)

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