2′-Dicyclohexylphosphino-2-methoxy-1-phenylnaphthalene

97%

Reagent Code: #169964
fingerprint
CAS Number 1309570-98-6

science Other reagents with same CAS 1309570-98-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 430.56 g/mol
Formula C₂₉H₃₅OP
badge Registry Numbers
MDL Number MFCD23704405
thermostat Physical Properties
Melting Point 155-160 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Widely used as a ligand in palladium-catalyzed cross-coupling reactions, this compound enhances catalytic efficiency and stability. It is particularly effective in Suzuki-Miyaura and Buchwald-Hartwig aminations, where it enables coupling under mild conditions with high yields. Its steric bulk and electron-rich phosphine group facilitate oxidative addition and prevent catalyst deactivation. Commonly employed in pharmaceutical synthesis and materials science, it supports the formation of carbon-carbon and carbon-heteroatom bonds in complex molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,920.00
inventory 250mg
10-20 days ฿14,220.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2′-Dicyclohexylphosphino-2-methoxy-1-phenylnaphthalene
No image available

Widely used as a ligand in palladium-catalyzed cross-coupling reactions, this compound enhances catalytic efficiency and stability. It is particularly effective in Suzuki-Miyaura and Buchwald-Hartwig aminations, where it enables coupling under mild conditions with high yields. Its steric bulk and electron-rich phosphine group facilitate oxidative addition and prevent catalyst deactivation. Commonly employed in pharmaceutical synthesis and materials science, it supports the formation of carbon-carbon and

Widely used as a ligand in palladium-catalyzed cross-coupling reactions, this compound enhances catalytic efficiency and stability. It is particularly effective in Suzuki-Miyaura and Buchwald-Hartwig aminations, where it enables coupling under mild conditions with high yields. Its steric bulk and electron-rich phosphine group facilitate oxidative addition and prevent catalyst deactivation. Commonly employed in pharmaceutical synthesis and materials science, it supports the formation of carbon-carbon and carbon-heteroatom bonds in complex molecules.

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...