2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole

97%

Reagent Code: #68770
fingerprint
CAS Number 1067883-58-2

science Other reagents with same CAS 1067883-58-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 403.54 g/mol
Formula C₂₇H₃₄NP
badge Registry Numbers
MDL Number MFCD16995285
thermostat Physical Properties
Melting Point 183 °C
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This compound is primarily utilized as a ligand in various catalytic processes, particularly in transition metal-catalyzed reactions. Its structure, featuring a dicyclohexylphosphino group and an indole moiety, makes it effective in stabilizing metal centers and enhancing catalytic activity. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it facilitates the formation of carbon-carbon bonds. Additionally, it finds use in asymmetric synthesis, contributing to the production of chiral molecules in pharmaceutical and fine chemical industries. Its robust performance in harsh reaction conditions further broadens its applicability in industrial and academic research settings.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,900.00
inventory 1g
10-20 days ฿25,740.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole
No image available

This compound is primarily utilized as a ligand in various catalytic processes, particularly in transition metal-catalyzed reactions. Its structure, featuring a dicyclohexylphosphino group and an indole moiety, makes it effective in stabilizing metal centers and enhancing catalytic activity. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it facilitates the formation of carbon-carbon bonds. Additionally, it finds use in asymmetric synthesis, contributing

This compound is primarily utilized as a ligand in various catalytic processes, particularly in transition metal-catalyzed reactions. Its structure, featuring a dicyclohexylphosphino group and an indole moiety, makes it effective in stabilizing metal centers and enhancing catalytic activity. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it facilitates the formation of carbon-carbon bonds. Additionally, it finds use in asymmetric synthesis, contributing to the production of chiral molecules in pharmaceutical and fine chemical industries. Its robust performance in harsh reaction conditions further broadens its applicability in industrial and academic research settings.

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...