(2R)-2-[(Diphenylphosphino)methyl]pyrrolidine

≥95%,≥99%e.e.

Reagent Code: #59649
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CAS Number 428514-91-4

science Other reagents with same CAS 428514-91-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.3 g/mol
Formula C₁₇H₂₀NP
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions, which are essential in the synthesis of pharmaceuticals and fine chemicals. Its ability to induce high enantioselectivity makes it valuable in producing optically active compounds with specific stereochemistry. Additionally, it is employed in academic and industrial research to develop new catalytic processes and optimize existing ones for improved efficiency and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,760.00
inventory 1g
10-20 days ฿74,910.00

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(2R)-2-[(Diphenylphosphino)methyl]pyrrolidine
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions, which are essential in the synthesis of pharmaceuticals and fine chemicals. Its ability to induce high enantioselectivity makes it valuable in producing optically active compounds with specific stereochemistry. Additionally, it is e

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions, which are essential in the synthesis of pharmaceuticals and fine chemicals. Its ability to induce high enantioselectivity makes it valuable in producing optically active compounds with specific stereochemistry. Additionally, it is employed in academic and industrial research to develop new catalytic processes and optimize existing ones for improved efficiency and selectivity.

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