1,3-Dimesitylimidazolidin-2-ylidene

95%

Reagent Code: #176162
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CAS Number 173035-11-5

science Other reagents with same CAS 173035-11-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.45 g/mol
Formula C₂₁H₂₆N₂
badge Registry Numbers
MDL Number MFCD11973794
thermostat Physical Properties
Melting Point 85-100 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a highly sterically hindered N-heterocyclic carbene (NHC) ligand in organometallic catalysis. It stabilizes reactive metal centers in transition metal complexes, particularly in ruthenium-based olefin metathesis catalysts, enhancing their activity and longevity. Its bulky mesityl groups provide strong electron donation and prevent catalyst decomposition, making it valuable in ring-closing metathesis and polymerization reactions. Also employed in palladium-catalyzed cross-coupling reactions to improve catalyst stability under harsh conditions. Additionally, serves as a ligand in CO2 activation and small molecule fixation due to its strong sigma-donating ability.

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inventory 100mg
10-20 days ฿6,660.00

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1,3-Dimesitylimidazolidin-2-ylidene
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Used as a highly sterically hindered N-heterocyclic carbene (NHC) ligand in organometallic catalysis. It stabilizes reactive metal centers in transition metal complexes, particularly in ruthenium-based olefin metathesis catalysts, enhancing their activity and longevity. Its bulky mesityl groups provide strong electron donation and prevent catalyst decomposition, making it valuable in ring-closing metathesis and polymerization reactions. Also employed in palladium-catalyzed cross-coupling reactions to imp

Used as a highly sterically hindered N-heterocyclic carbene (NHC) ligand in organometallic catalysis. It stabilizes reactive metal centers in transition metal complexes, particularly in ruthenium-based olefin metathesis catalysts, enhancing their activity and longevity. Its bulky mesityl groups provide strong electron donation and prevent catalyst decomposition, making it valuable in ring-closing metathesis and polymerization reactions. Also employed in palladium-catalyzed cross-coupling reactions to improve catalyst stability under harsh conditions. Additionally, serves as a ligand in CO2 activation and small molecule fixation due to its strong sigma-donating ability.

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