(2R,3R)-4-(Anthracen-9-yl)-3-(tert-butyl)-2-ethyl-2,3-dihydrobenzo[d][1,3]oxaphosphole

≥97%

Reagent Code: #229324
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CAS Number 2565792-21-2

science Other reagents with same CAS 2565792-21-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 398.48 g/mol
Formula C₂₇H₂₇OP
thermostat Physical Properties
Boiling Point 540.9±50.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its rigid backbone and stereogenic centers enable high enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The anthracenyl group enhances π-stacking interactions, improving catalyst stability and selectivity. Effective in palladium- and rhodium-based catalytic systems for producing enantiomerically pure compounds.

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inventory 50mg
10-20 days ฿3,580.00

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(2R,3R)-4-(Anthracen-9-yl)-3-(tert-butyl)-2-ethyl-2,3-dihydrobenzo[d][1,3]oxaphosphole
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Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its rigid backbone and stereogenic centers enable high enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The anthracenyl group enhances π-stacking interactions, improving catalyst stability and selectivity. Effective in palladium- and rhodium-based catalytic systems for producing e

Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its rigid backbone and stereogenic centers enable high enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The anthracenyl group enhances π-stacking interactions, improving catalyst stability and selectivity. Effective in palladium- and rhodium-based catalytic systems for producing enantiomerically pure compounds.

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