di-tert-butyl((2R,3R)-3-(tert-butyl)-4-isopropoxy-2,3-dihydrobenzo[d][1,3]oxaphosphol-2-yl)phosphine oxide

97%, 99%ee

Reagent Code: #229155
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CAS Number 2545293-93-2

science Other reagents with same CAS 2545293-93-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 412.49 g/mol
Formula C₂₂H₃₈O₃P₂
thermostat Physical Properties
Boiling Point 537.4±50.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

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 phosphine oxide group can be reduced to the corresponding phosphine, which coordinates effectively with metals like palladium, rhodium, and ruthenium to form active catalytic species. Its steric bulk and electronic properties enhance catalyst stability and selectivity under various reaction conditions.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿17,590.00

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di-tert-butyl((2R,3R)-3-(tert-butyl)-4-isopropoxy-2,3-dihydrobenzo[d][1,3]oxaphosphol-2-yl)phosphine oxide
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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 phosphine oxide group can be reduced to the corresponding phosphine, which coordinates effectively with metals like palladium, rhodium, and ruthenium to form active catalyti

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 phosphine oxide group can be reduced to the corresponding phosphine, which coordinates effectively with metals like palladium, rhodium, and ruthenium to form active catalytic species. Its steric bulk and electronic properties enhance catalyst stability and selectivity under various reaction conditions.

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