(4R,5R)-4,5-Diphenyl-1,3-di-o-tolyl-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborate

98%

Reagent Code: #229431
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CAS Number 372517-13-0

science Other reagents with same CAS 372517-13-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 490.34 g/mol
Formula C₂₉H₂₇BF₄N₂
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 formation reactions. The steric bulk and electronic properties of the o-tolyl and diphenyl groups enhance stereoselectivity and catalyst stability. Commonly employed in organometallic complexes with ruthenium, rhodium, or palladium for high enantiomeric excess in pharmaceutical and fine chemical synthesis. Also applied in the development of chiral ionic liquids and as a ligand in homogeneous catalysis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿12,010.00
250mg
10-20 days ฿20,420.00
(4R,5R)-4,5-Diphenyl-1,3-di-o-tolyl-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 formation reactions. The steric bulk and electronic properties of the o-tolyl and diphenyl groups enhance stereoselectivity and catalyst stability. Commonly employed in organometallic complexes with ruthenium, rhodium, or palladium for high enantiomeric excess in pharmaceutical and fine chemical synthesis. Also appli

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. The steric bulk and electronic properties of the o-tolyl and diphenyl groups enhance stereoselectivity and catalyst stability. Commonly employed in organometallic complexes with ruthenium, rhodium, or palladium for high enantiomeric excess in pharmaceutical and fine chemical synthesis. Also applied in the development of chiral ionic liquids and as a ligand in homogeneous catalysis.

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