4-(2-(Di(adamantan-1-yl)phosphino)phenyl)morpholine

98%

Reagent Code: #68332
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CAS Number 1237588-12-3

science Other reagents with same CAS 1237588-12-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 463.63 g/mol
Formula C₃₀H₄₂NOP
badge Registry Numbers
MDL Number MFCD17018759
inventory_2 Storage & Handling
Storage Inert gas, 2-8°C

description Product Description

This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, featuring adamantyl groups and a morpholine moiety, enhances stability and selectivity in various catalytic applications. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Additionally, its steric and electronic properties make it suitable for asymmetric catalysis, contributing to the synthesis of chiral molecules in pharmaceuticals and fine chemicals. The ligand’s robustness under harsh reaction conditions further expands its utility in industrial and academic research settings.

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Test Parameter Specification
Appearance White to off-white solid
Purity 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿25,800.00
inventory 100mg
10-20 days ฿3,880.00
inventory 250mg
10-20 days ฿6,880.00

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4-(2-(Di(adamantan-1-yl)phosphino)phenyl)morpholine
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This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, featuring adamantyl groups and a morpholine moiety, enhances stability and selectivity in various catalytic applications. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Additionally, its steric and electronic properties make

This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, featuring adamantyl groups and a morpholine moiety, enhances stability and selectivity in various catalytic applications. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Additionally, its steric and electronic properties make it suitable for asymmetric catalysis, contributing to the synthesis of chiral molecules in pharmaceuticals and fine chemicals. The ligand’s robustness under harsh reaction conditions further expands its utility in industrial and academic research settings.

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