1,3-Bis((R)-1-(naphthalen-1-yl)ethyl)-1H-imidazol-3-ium chloride

97%

Reagent Code: #152971
fingerprint
CAS Number 186354-48-3

science Other reagents with same CAS 186354-48-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 412.95 g/mol
Formula C₂₇H₂₅ClN₂
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-couplings, hydrogenations, and cyclizations. The bulky naphthyl groups enhance stereoselectivity by creating a well-defined chiral environment around the metal center. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is required. Also utilized in organocatalytic processes and as a ligand scaffold in the development of new catalytic systems.

shopping_cart Available Sizes & Pricing

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

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1,3-Bis((R)-1-(naphthalen-1-yl)ethyl)-1H-imidazol-3-ium chloride
No image available

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-couplings, hydrogenations, and cyclizations. The bulky naphthyl groups enhance stereoselectivity by creating a well-defined chiral environment around the metal center. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is required. Also uti

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-couplings, hydrogenations, and cyclizations. The bulky naphthyl groups enhance stereoselectivity by creating a well-defined chiral environment around the metal center. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is required. Also utilized in organocatalytic processes and as a ligand scaffold in the development of new catalytic systems.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...