656577
1,3-Diisopropylimidazolium chloride
97%
Synonym(s):
N,N′-(Isopropyl)imidazolium chloride
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About This Item
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Quality Level
Assay
97%
form
solid
reaction suitability
reagent type: catalyst
greener alternative product characteristics
Catalysis
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Greener Alternative Product
mp
182-186 °C
greener alternative category
SMILES string
[Cl-].CC(C)n1cc[n+](c1)C(C)C
InChI
1S/C9H17N2.ClH/c1-8(2)10-5-6-11(7-10)9(3)4;/h5-9H,1-4H3;1H/q+1;/p-1
InChI key
DOFXKPAOJLLPII-UHFFFAOYSA-M
General description
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
Application
1,3-Diisopropylimidazolium chloride may be used to prepare:
- 1,3-Diisopropylimidazole-2-thione by reacting with sulfur in the presence of potassium carbonate.
- (C9H7)NiCl(1,3-diisopropylimidazol-2- ylidene) by reacting with bis-indenyl nickel-(II).
- Ruthenium N-heterocyclic carbene complexes, which are efficient catalysts for the amidation of primary alcohols and amines.
Ligand for ruthenium-catalyzed greener amide bond formation by dehydrogenative coupling of amines and alcohols.
Amide Synthesis from Alcohols and Amines by the Extrusion of Dihydrogen
Amide Synthesis from Alcohols and Amines by the Extrusion of Dihydrogen
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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