(4S,5S)-1,3-Bis(2-(methoxymethyl)phenyl)-4,5-diphenyl-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborate

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Reagent Code: #233237
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CAS Number 1033618-53-9

science Other reagents with same CAS 1033618-53-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 550.4 g/mol
Formula C₃₁H₃₁BF₄N₂O₂
thermostat Physical Properties
Melting Point 155-157 °C
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral N-heterocyclic carbene (NHC) precursor in asymmetric catalysis. It plays a key role in enantioselective transformations such as hydrogenation, cyclopropanation, and C–C bond-forming reactions. The ligand derived from this compound coordinates to transition metals like palladium, rhodium, and ruthenium, enabling high stereocontrol in the synthesis of pharmaceuticals and fine chemicals. Its steric bulk and electronic properties enhance catalyst stability and selectivity. Commonly applied in academic and industrial research for developing chiral molecules with high optical purity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,450.00
inventory 250mg
10-20 days ฿19,480.00

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(4S,5S)-1,3-Bis(2-(methoxymethyl)phenyl)-4,5-diphenyl-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborate
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Used as a chiral N-heterocyclic carbene (NHC) precursor in asymmetric catalysis. It plays a key role in enantioselective transformations such as hydrogenation, cyclopropanation, and C–C bond-forming reactions. The ligand derived from this compound coordinates to transition metals like palladium, rhodium, and ruthenium, enabling high stereocontrol in the synthesis of pharmaceuticals and fine chemicals. Its steric bulk and electronic properties enhance catalyst stability and selectivity. Commonly applied i

Used as a chiral N-heterocyclic carbene (NHC) precursor in asymmetric catalysis. It plays a key role in enantioselective transformations such as hydrogenation, cyclopropanation, and C–C bond-forming reactions. The ligand derived from this compound coordinates to transition metals like palladium, rhodium, and ruthenium, enabling high stereocontrol in the synthesis of pharmaceuticals and fine chemicals. Its steric bulk and electronic properties enhance catalyst stability and selectivity. Commonly applied in academic and industrial research for developing chiral molecules with high optical purity.

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