Dicyclohexyl(2,6-diisopropoxyphenyl)phosphine

98%

Reagent Code: #167751
fingerprint
CAS Number 1268824-69-6

science Other reagents with same CAS 1268824-69-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 390.54 g/mol
Formula C₂₄H₃₉O₂P
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a ligand in palladium-catalyzed cross-coupling reactions, particularly in Buchwald–Hartwig amination and Suzuki–Miyaura coupling. Its steric bulk and electron-rich nature enhance catalyst stability and reactivity, enabling efficient C–N and C–C bond formation under mild conditions. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where high selectivity and functional group tolerance are required. Also effective in catalyzing reactions involving challenging substrates such as aryl chlorides.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿12,880.00
inventory 1g
10-20 days ฿32,770.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Dicyclohexyl(2,6-diisopropoxyphenyl)phosphine
No image available

Used as a ligand in palladium-catalyzed cross-coupling reactions, particularly in Buchwald–Hartwig amination and Suzuki–Miyaura coupling. Its steric bulk and electron-rich nature enhance catalyst stability and reactivity, enabling efficient C–N and C–C bond formation under mild conditions. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where high selectivity and functional group tolerance are required. Also effective in catalyzing reactions involving challenging substrates s

Used as a ligand in palladium-catalyzed cross-coupling reactions, particularly in Buchwald–Hartwig amination and Suzuki–Miyaura coupling. Its steric bulk and electron-rich nature enhance catalyst stability and reactivity, enabling efficient C–N and C–C bond formation under mild conditions. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where high selectivity and functional group tolerance are required. Also effective in catalyzing reactions involving challenging substrates such as aryl chlorides.

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...