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

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Reagent Code: #153414
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CAS Number 569658-93-1

science Other reagents with same CAS 569658-93-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 364.19 g/mol
Formula C₁₉H₂₁BF₄N₂
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-forming reactions. The compound’s bulky chiral groups help induce high stereoselectivity when coordinated to transition metals like ruthenium, rhodium, or palladium. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where control over stereochemistry is critical. Its tetrafluoroborate salt form enhances stability and handling in air-sensitive reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,850.00
inventory 250mg
10-20 days ฿6,570.00
inventory 1g
10-20 days ฿21,200.00

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1,3-Bis((R)-1-phenylethyl)-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-forming reactions. The compound’s bulky chiral groups help induce high stereoselectivity when coordinated to transition metals like ruthenium, rhodium, or palladium. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where control over stereochemistry is critical. Its tetrafluoroborat

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-forming reactions. The compound’s bulky chiral groups help induce high stereoselectivity when coordinated to transition metals like ruthenium, rhodium, or palladium. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where control over stereochemistry is critical. Its tetrafluoroborate salt form enhances stability and handling in air-sensitive reactions.

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