(Oxybis(2,1-phenylene))bis(bis(4-methoxy-3,5-dimethylphenyl)phosphine)

97%

Reagent Code: #222283
fingerprint
CAS Number 2054939-79-4

science Other reagents with same CAS 2054939-79-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 770.87 g/mol
Formula C₄₈H₅₂O₅P₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a specialized ligand in palladium-catalyzed cross-coupling reactions, enabling efficient formation of carbon-carbon bonds in complex organic synthesis. Its sterically hindered, electron-rich structure enhances catalyst stability and selectivity, particularly in challenging transformations such as aryl-aryl couplings and late-stage functionalization of pharmaceuticals. Commonly applied in the development of advanced intermediates for agrochemicals, pharmaceuticals, and materials science where high catalytic efficiency and functional group tolerance are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿11,750.00
inventory 100mg
10-20 days ฿19,970.00
inventory 250mg
10-20 days ฿33,940.00
inventory 1g
10-20 days ฿106,590.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(Oxybis(2,1-phenylene))bis(bis(4-methoxy-3,5-dimethylphenyl)phosphine)
No image available

Used as a specialized ligand in palladium-catalyzed cross-coupling reactions, enabling efficient formation of carbon-carbon bonds in complex organic synthesis. Its sterically hindered, electron-rich structure enhances catalyst stability and selectivity, particularly in challenging transformations such as aryl-aryl couplings and late-stage functionalization of pharmaceuticals. Commonly applied in the development of advanced intermediates for agrochemicals, pharmaceuticals, and materials science where high

Used as a specialized ligand in palladium-catalyzed cross-coupling reactions, enabling efficient formation of carbon-carbon bonds in complex organic synthesis. Its sterically hindered, electron-rich structure enhances catalyst stability and selectivity, particularly in challenging transformations such as aryl-aryl couplings and late-stage functionalization of pharmaceuticals. Commonly applied in the development of advanced intermediates for agrochemicals, pharmaceuticals, and materials science where high catalytic efficiency and functional group tolerance are required.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...