1,3-Bis((R)-1-phenylpropyl)-1H-imidazol-3-ium tetrafluoroborate

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Reagent Code: #229295
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CAS Number 2757082-93-0

science Other reagents with same CAS 2757082-93-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 392.25 g/mol
Formula C₂₁H₂₅BF₄N₂
inventory_2 Storage & Handling
Storage Room temperature, 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, allylic alkylation, and ring-opening reactions, where high stereocontrol is required. The compound’s chiral imidazolium structure enables the formation of well-defined metal-NHC complexes, particularly with palladium, ruthenium, and iridium, enhancing catalytic efficiency and enantioselectivity. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing to produce single-enantiomer compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,860.00
inventory 250mg
10-20 days ฿6,560.00
inventory 1g
10-20 days ฿17,730.00

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1,3-Bis((R)-1-phenylpropyl)-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, allylic alkylation, and ring-opening reactions, where high stereocontrol is required. The compound’s chiral imidazolium structure enables the formation of well-defined metal-NHC complexes, particularly with palladium, ruthenium, and iridium, enhancing catalytic efficiency and enantioselectivity. Commonly applied in pharmaceutical synthesis and fi

Used as a chiral N-heterocyclic carbene (NHC) precursor in asymmetric catalysis. It plays a key role in enantioselective transformations, such as hydrogenation, allylic alkylation, and ring-opening reactions, where high stereocontrol is required. The compound’s chiral imidazolium structure enables the formation of well-defined metal-NHC complexes, particularly with palladium, ruthenium, and iridium, enhancing catalytic efficiency and enantioselectivity. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing to produce single-enantiomer compounds.

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