Tris(4-trifluoromethylphenyl)phosphine

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Reagent Code: #121808
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Alias Tris(4-trifluoromethylphenyl)phosphine
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CAS Number 13406-29-6

science Other reagents with same CAS 13406-29-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 466.28 g/mol
Formula CF₃C₆H₄₃P
badge Registry Numbers
MDL Number MFCD00058883
thermostat Physical Properties
Melting Point 70-75 °C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Tris(4-trifluoromethylphenyl)phosphine is primarily utilized as a ligand in organometallic chemistry and catalysis. Its electron-withdrawing trifluoromethyl groups enhance the stability and reactivity of metal complexes, making it valuable in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions. It is also employed in the synthesis of fine chemicals and pharmaceuticals, where precise control over reaction pathways is essential. Additionally, its unique properties make it suitable for use in materials science, particularly in the development of advanced polymers and coatings with specific electronic or chemical resistance characteristics.

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Test Parameter Specification
Melting Point 72-76
Purity (GC) 98.5-100
Appearance White or light yellow powder
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿11,090.00
inventory 1g
10-20 days ฿2,600.00
inventory 250mg
10-20 days ฿870.00

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Tris(4-trifluoromethylphenyl)phosphine
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Tris(4-trifluoromethylphenyl)phosphine is primarily utilized as a ligand in organometallic chemistry and catalysis. Its electron-withdrawing trifluoromethyl groups enhance the stability and reactivity of metal complexes, making it valuable in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions. It is also employed in the synthesis of fine chemicals and pharmaceuticals, where precise control over reaction pathways is essential. Additionally, its unique properties make it suitable for use i

Tris(4-trifluoromethylphenyl)phosphine is primarily utilized as a ligand in organometallic chemistry and catalysis. Its electron-withdrawing trifluoromethyl groups enhance the stability and reactivity of metal complexes, making it valuable in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions. It is also employed in the synthesis of fine chemicals and pharmaceuticals, where precise control over reaction pathways is essential. Additionally, its unique properties make it suitable for use in materials science, particularly in the development of advanced polymers and coatings with specific electronic or chemical resistance characteristics.

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