Tri(2-furyl)phosphine

98%

Reagent Code: #68875
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Alias Tris(2-furyl)phosphine
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CAS Number 5518-52-5

science Other reagents with same CAS 5518-52-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.17 g/mol
Formula C₁₂H₉O₃P
badge Registry Numbers
MDL Number MFCD00151857
thermostat Physical Properties
Melting Point 59-64 °C(lit.)
Boiling Point 136 °C4 mm Hg(lit.)
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Tri(2-furyl)phosphine is primarily used as a ligand in coordination chemistry and catalysis. It is particularly valuable in the synthesis of organometallic compounds, where it facilitates the stabilization of metal centers and enhances catalytic activity. This compound is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are crucial for forming carbon-carbon bonds in organic synthesis. Its unique electronic properties make it effective in asymmetric catalysis, enabling the production of chiral molecules with high enantioselectivity. Additionally, tri(2-furyl)phosphine is utilized in the development of materials science, particularly in the creation of metal-organic frameworks (MOFs) and other advanced materials. Its versatility and ability to modify metal reactivity make it a key component in both academic research and industrial applications.

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Test Parameter Specification
Melting point 61-64
Purity (GC) 98-100%
Appearance White to off-white powder, crystals and/or chunks
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,020.00
inventory 5g
10-20 days ฿2,860.00
inventory 25g
10-20 days ฿10,580.00
inventory 250mg
10-20 days ฿540.00

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Tri(2-furyl)phosphine
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Tri(2-furyl)phosphine is primarily used as a ligand in coordination chemistry and catalysis. It is particularly valuable in the synthesis of organometallic compounds, where it facilitates the stabilization of metal centers and enhances catalytic activity. This compound is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are crucial for forming carbon-carbon bonds in organic synthesis. Its unique electronic properties make it effective in asymmetric catalysis, e

Tri(2-furyl)phosphine is primarily used as a ligand in coordination chemistry and catalysis. It is particularly valuable in the synthesis of organometallic compounds, where it facilitates the stabilization of metal centers and enhances catalytic activity. This compound is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are crucial for forming carbon-carbon bonds in organic synthesis. Its unique electronic properties make it effective in asymmetric catalysis, enabling the production of chiral molecules with high enantioselectivity. Additionally, tri(2-furyl)phosphine is utilized in the development of materials science, particularly in the creation of metal-organic frameworks (MOFs) and other advanced materials. Its versatility and ability to modify metal reactivity make it a key component in both academic research and industrial applications.

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