(4R,5R)-1,3-Dimesityl-4,5-diphenyl-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborate

98%

Reagent Code: #231799
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CAS Number 372517-11-8

science Other reagents with same CAS 372517-11-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 546.45 g/mol
Formula C₃₃H₃₅BF₄N₂
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Widely used as a precursor to N-heterocyclic carbene (NHC) ligands in organometallic catalysis. Its steric bulk and electron-donating properties make it ideal for stabilizing reactive metal centers in cross-coupling reactions, olefin metathesis, and hydrogenation processes. Commonly employed in the synthesis of ruthenium- or palladium-based catalysts where enhanced stability and activity are required. The tetrafluoroborate counterion supports solubility in polar organic solvents, facilitating its use in homogeneous reaction systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,460.00
inventory 250mg
10-20 days ฿10,930.00
inventory 1g
10-20 days ฿32,950.00
(4R,5R)-1,3-Dimesityl-4,5-diphenyl-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborate
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Widely used as a precursor to N-heterocyclic carbene (NHC) ligands in organometallic catalysis. Its steric bulk and electron-donating properties make it ideal for stabilizing reactive metal centers in cross-coupling reactions, olefin metathesis, and hydrogenation processes. Commonly employed in the synthesis of ruthenium- or palladium-based catalysts where enhanced stability and activity are required. The tetrafluoroborate counterion supports solubility in polar organic solvents, facilitating its use in

Widely used as a precursor to N-heterocyclic carbene (NHC) ligands in organometallic catalysis. Its steric bulk and electron-donating properties make it ideal for stabilizing reactive metal centers in cross-coupling reactions, olefin metathesis, and hydrogenation processes. Commonly employed in the synthesis of ruthenium- or palladium-based catalysts where enhanced stability and activity are required. The tetrafluoroborate counterion supports solubility in polar organic solvents, facilitating its use in homogeneous reaction systems.

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