(2R,4R)-Pentane-2,4-diylbis[bis(4-dimethylaminophenyl)phosphine]

≥90.0%(qNMR)

Reagent Code: #229077
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CAS Number 132957-17-6

science Other reagents with same CAS 132957-17-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 612.78 g/mol
Formula C₃₇H₅₀N₄P₂
thermostat Physical Properties
Melting Point 175 °C
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a chiral bidentate phosphine ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation, allylic alkylation, and cross-coupling transformations. Its stereochemistry enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The electron-rich dimethylamino groups stabilize metal complexes and improve catalytic efficiency. Commonly employed with rhodium, ruthenium, or palladium complexes for high enantiomeric excess in asymmetric synthesis.

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inventory 100mg
10-20 days ฿16,730.00

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(2R,4R)-Pentane-2,4-diylbis[bis(4-dimethylaminophenyl)phosphine]
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Used as a chiral bidentate phosphine ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation, allylic alkylation, and cross-coupling transformations. Its stereochemistry enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The electron-rich dimethylamino groups stabilize metal complexes and improve catalytic efficiency. Commonly employed with rhodium, ruthenium, or palladium complexes fo

Used as a chiral bidentate phosphine ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation, allylic alkylation, and cross-coupling transformations. Its stereochemistry enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The electron-rich dimethylamino groups stabilize metal complexes and improve catalytic efficiency. Commonly employed with rhodium, ruthenium, or palladium complexes for high enantiomeric excess in asymmetric synthesis.

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