Tris(1-adamantyl)phosphine

≥98%

Reagent Code: #68874
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CAS Number 897665-73-5

science Other reagents with same CAS 897665-73-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 436.65 g/mol
Formula C₃₀H₄₅P
badge Registry Numbers
MDL Number MFCD30475335
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Tris(1-adamantyl)phosphine is primarily utilized in the field of organic synthesis and catalysis. Its bulky structure makes it an effective ligand in transition metal-catalyzed reactions, particularly in cross-coupling reactions, where it enhances selectivity and efficiency. The compound is also employed in the development of advanced materials, such as polymers and coordination complexes, due to its ability to stabilize reactive intermediates. Additionally, it finds use in research focused on phosphine chemistry, where its unique steric properties are studied for designing novel catalysts and understanding reaction mechanisms.

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Test Parameter Specification
Appearance White to Light Yellow Solid
Purity (%) 98-100
LC-MS Conforms to Structure
Infrared spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,301.00
inventory 1g
10-20 days ฿15,930.00
inventory 100mg
10-20 days ฿3,519.00

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Tris(1-adamantyl)phosphine
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Tris(1-adamantyl)phosphine is primarily utilized in the field of organic synthesis and catalysis. Its bulky structure makes it an effective ligand in transition metal-catalyzed reactions, particularly in cross-coupling reactions, where it enhances selectivity and efficiency. The compound is also employed in the development of advanced materials, such as polymers and coordination complexes, due to its ability to stabilize reactive intermediates. Additionally, it finds use in research focused on phosphine

Tris(1-adamantyl)phosphine is primarily utilized in the field of organic synthesis and catalysis. Its bulky structure makes it an effective ligand in transition metal-catalyzed reactions, particularly in cross-coupling reactions, where it enhances selectivity and efficiency. The compound is also employed in the development of advanced materials, such as polymers and coordination complexes, due to its ability to stabilize reactive intermediates. Additionally, it finds use in research focused on phosphine chemistry, where its unique steric properties are studied for designing novel catalysts and understanding reaction mechanisms.

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