(S)-2-diphenyphosphino,2'-hydroxyl-1,1'-binaphthyl

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Reagent Code: #57540
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CAS Number 144868-15-5

science Other reagents with same CAS 144868-15-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 454.51 g/mol
Formula C₃₂H₂₃OP
thermostat Physical Properties
Boiling Point 602.3±43.0 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective hydrogenation, where it helps produce chiral molecules with high enantiomeric purity, essential in the synthesis of pharmaceuticals and fine chemicals. Its application extends to carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation and cross-coupling reactions, enabling the production of complex organic compounds with precise stereochemistry. Additionally, it is employed in the synthesis of chiral ligands and catalysts, further expanding its utility in organic synthesis and industrial processes.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿13,050.00
inventory 100mg
10-20 days ฿39,222.00

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(S)-2-diphenyphosphino,2'-hydroxyl-1,1'-binaphthyl
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This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective hydrogenation, where it helps produce chiral molecules with high enantiomeric purity, essential in the synthesis of pharmaceuticals and fine chemicals. Its application extends to carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation and cross-coupling reactions, enabling the production of complex organic compounds

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective hydrogenation, where it helps produce chiral molecules with high enantiomeric purity, essential in the synthesis of pharmaceuticals and fine chemicals. Its application extends to carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation and cross-coupling reactions, enabling the production of complex organic compounds with precise stereochemistry. Additionally, it is employed in the synthesis of chiral ligands and catalysts, further expanding its utility in organic synthesis and industrial processes.

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