Tri-1-naphthylphosphine

97%

Reagent Code: #121804
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Alias Tris(1-naphthyl)phosphine
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CAS Number 3411-48-1

science Other reagents with same CAS 3411-48-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 412.46 g/mol
Formula C₁₀H₇₃P
badge Registry Numbers
MDL Number MFCD00046400
thermostat Physical Properties
Melting Point 265 °C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Tri-1-naphthylphosphine is primarily used as a ligand in coordination chemistry and catalysis. Its bulky structure makes it effective in stabilizing metal complexes, particularly in transition metal-catalyzed reactions. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it enhances selectivity and efficiency. Additionally, it finds applications in the synthesis of organic compounds, including pharmaceuticals and fine chemicals, due to its ability to facilitate challenging transformations. Its use in asymmetric catalysis is also notable, as it can induce chirality in the resulting products.

format_list_bulleted Product Specification

Test Parameter Specification
Melting Point 261-265
Purity (HPLC) 97-100%
Appearance White to Tan Solid
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,260.00
inventory 5g
10-20 days ฿4,800.00
inventory 25g
10-20 days ฿19,890.00

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Tri-1-naphthylphosphine
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Tri-1-naphthylphosphine is primarily used as a ligand in coordination chemistry and catalysis. Its bulky structure makes it effective in stabilizing metal complexes, particularly in transition metal-catalyzed reactions. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it enhances selectivity and efficiency. Additionally, it finds applications in the synthesis of organic compounds, including pharmaceuticals and fine chemicals, due to its ability to facilit

Tri-1-naphthylphosphine is primarily used as a ligand in coordination chemistry and catalysis. Its bulky structure makes it effective in stabilizing metal complexes, particularly in transition metal-catalyzed reactions. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it enhances selectivity and efficiency. Additionally, it finds applications in the synthesis of organic compounds, including pharmaceuticals and fine chemicals, due to its ability to facilitate challenging transformations. Its use in asymmetric catalysis is also notable, as it can induce chirality in the resulting products.

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