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  • 656623 - 1,3-Bis-(2,6-diisopropylphenyl)imidazolinium chloride

Aldrich

1,3-Bis-(2,6-diisopropylphenyl)imidazolinium chloride

656623 -

97%

DOWNLOAD MSDS (PDF)

Synonym: N,N′-(2,6-Diisopropylphenyl)dihydroimidazolium chloride

1,3-Bis-(2,6-diisopropylphenyl)imidazolinium chloride 97%
#

Properties

Related CategoriesCatalysis and Inorganic Chemistry, Chemical Synthesis, NHC Compounds
assay97%
mp289-293 °C(lit.)

Description

Packaging

1, 5 g in glass btl

Application

N-Heterocyclic Carbene Ligands

Price and Availability


Documents

Certificate of Analysis

Certificate of Origin

ChemFiles Vol 5 No 10 (1 MB )
Structure Search
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Safety Information

SymbolGHS07  GHS07
Signal wordWarning
Hazard statementsH315-H319-H335
Precautionary statementsP261-P305 + P351 + P338
Personal Protective Equipmentdust mask type N95 (US), Eyeshields, Gloves
Hazard CodesXi
Risk Statements36/37/38
Safety Statements26-36
WGK Germany3
Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Articles

N-Heterocyclic Carbene (NHC) Ligands

Rapid progress in cross-coupling reactions of unactivated substrates catalyzed by metal complexes has transformed the chemical market-place through introduction of an extensive library of achiral and...
ChemFiles Volume 5 Article 10
Keywords: Aminations, Arylations, Catalysis, Coupling reactions, Cross couplings, Cyclizations, Eliminations, Hydrogenations, Ligands, Metathesis, Oxidative additions, Reductive eliminations

Related Content

N-Heterocyclic Carbene Ligands in Chemical Synthesis

Rapid progress in cross-coupling reactions of unactivated substrates catalyzed by metal complexes has transformed the chemical marketplace through introduction of an extensive library of achiral and ...

References

Synlett, 366, (2006)

Andrus, M. B.; Song, C.; Zhang J. Org. Chem. 4, 2079, (2002)

Sprengers, J. W.; Wassenaar, J. et al. Angew. Chem. Int. Ed. Engl. 44, 2026, (2005)

Wang, L.; Thai, K.; Gravel, M. Org. Lett. 11, 891, (2009) Abstract


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