(4S,5S)-1,3-Bis(2,6-diethylphenyl)-4,5-diphenyl-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborate

97%

Reagent Code: #233464
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CAS Number 1033618-45-9

science Other reagents with same CAS 1033618-45-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 574.51 g/mol
Formula C₃₅H₃₉BF₄N₂
thermostat Physical Properties
Melting Point 258-261 °C(Solv: ethyl ether (60-29-7); chloroform (67-66-3))
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Widely 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 formation reactions. Due to its steric bulk and well-defined chiral environment, it helps achieve high enantioselectivity when coordinated to transition metals like ruthenium, rhodium, or palladium. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where control over stereochemistry is critical. Its tetrafluoroborate salt form enhances stability and handling in air-sensitive reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,210.00
inventory 250mg
10-20 days ฿22,470.00
(4S,5S)-1,3-Bis(2,6-diethylphenyl)-4,5-diphenyl-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborate
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Widely 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 formation reactions. Due to its steric bulk and well-defined chiral environment, it helps achieve high enantioselectivity when coordinated to transition metals like ruthenium, rhodium, or palladium. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where control over stereochemistry is c

Widely 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 formation reactions. Due to its steric bulk and well-defined chiral environment, it helps achieve high enantioselectivity when coordinated to transition metals like ruthenium, rhodium, or palladium. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where control over stereochemistry is critical. Its tetrafluoroborate salt form enhances stability and handling in air-sensitive reactions.

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