1,3-Bis((S)-1-(naphthalen-1-yl)ethyl)-1H-imidazol-3-ium tetrafluoroborate

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Reagent Code: #153416
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CAS Number 569658-97-5

science Other reagents with same CAS 569658-97-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 464.31 g/mol
Formula C₂₇H₂₅BF₄N₂
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, particularly in transition metal-catalyzed reactions such as asymmetric cross-coupling, hydrogenation, and cyclopropanation. The compound’s bulky naphthyl groups enhance stereoselectivity by creating a well-defined chiral environment around the metal center. It is especially valuable in the synthesis of optically active pharmaceuticals and fine chemicals where high enantiomeric excess is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,120.00
inventory 250mg
10-20 days ฿12,160.00
inventory 1g
10-20 days ฿37,290.00

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1,3-Bis((S)-1-(naphthalen-1-yl)ethyl)-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, particularly in transition metal-catalyzed reactions such as asymmetric cross-coupling, hydrogenation, and cyclopropanation. The compound’s bulky naphthyl groups enhance stereoselectivity by creating a well-defined chiral environment around the metal center. It is especially valuable in the synthesis of optically active pharmaceuticals and fine chemicals where high ena

Used as a chiral N-heterocyclic carbene (NHC) precursor in asymmetric catalysis. It plays a key role in enantioselective transformations, particularly in transition metal-catalyzed reactions such as asymmetric cross-coupling, hydrogenation, and cyclopropanation. The compound’s bulky naphthyl groups enhance stereoselectivity by creating a well-defined chiral environment around the metal center. It is especially valuable in the synthesis of optically active pharmaceuticals and fine chemicals where high enantiomeric excess is required.

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