04124
1-(3-Cyanopropyl)-3-methylimidazolium chloride
Task Specific Ionic Liquid (TSIL), ≥98.5% (T)
Synonym(s):
1-Methyl-3-(3-cyanopropyl)imidazolium chloride
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About This Item
Quality Level
Assay
≥98.5% (T)
≥98.5% (elemental analysis, N)
form
powder
impurities
≤0.5% water
SMILES string
[Cl-].C[n+]1ccn(CCCC#N)c1
InChI
1S/C8H12N3.ClH/c1-10-6-7-11(8-10)5-3-2-4-9;/h6-8H,2-3,5H2,1H3;1H/q+1;/p-1
InChI key
HGPSWUJKMXIBKA-UHFFFAOYSA-M
General description
Nitrile-functionalized ionic liquid showing superior characteristics in Suzuki and Stille coupling reactions.
Application
1-(3-Cyanopropyl)-3-methylimidazolium chloride can be used:
- To prepare ionic polymers stabilized with palladium nanoparticle catalysts, which are applicable in the hydrogenation of alkenes and arenes.
- As a solvent in the synthesis of substituted 4-arylthio-1,2-oxazoles by reacting different aryl iodides with acetylenic oximes in the presence of Pd-NHC catalyst.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Aqueous-phase hydrogenation of alkenes and arenes: The growing role of nanoscale catalysts
Catalysis Today, 247, 96-103 (2015)
Recent advances in sulfuration chemistry enabled by bunte salts
Aldrichimica Acta, 53(1), 19-19 (2020)
Journal of the American Chemical Society, 126(48), 15876-15882 (2004-12-02)
A series of relatively low-cost ionic liquids, based on the N-butyronitrile pyridinium cation [C(3)CNpy](+), designed to improve catalyst retention, have been prepared and evaluated in Suzuki and Stille coupling reactions. Depending on the nature of the anion, these salts react
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