Tris(4-fluorophenyl)phosphine

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Reagent Code: #68866
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Alias Tris(4-fluorophenyl)phosphine
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CAS Number 18437-78-0

science Other reagents with same CAS 18437-78-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.26 g/mol
Formula FC₆H₄₃P
badge Registry Numbers
MDL Number MFCD00013553
thermostat Physical Properties
Melting Point 79-83 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Tris(4-fluorophenyl)phosphine is widely used as a ligand in coordination chemistry and catalysis, particularly in transition metal-catalyzed reactions. Its electron-withdrawing fluorine substituents enhance the stability and reactivity of metal complexes, making it valuable in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. It also finds application in the synthesis of organic semiconductors and optoelectronic materials due to its ability to modify electronic properties. Additionally, it serves as a precursor in the preparation of phosphine-based polymers and advanced materials for use in sensors and coatings. Its role in asymmetric catalysis further highlights its importance in producing chiral compounds for pharmaceuticals and fine chemicals.

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Test Parameter Specification
Melting point 79-83
Purity (GC) 98-100%
Appearance White to off-white or light yellow powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿650.00
inventory 25g
10-20 days ฿2,990.00
inventory 100g
10-20 days ฿11,300.00

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Tris(4-fluorophenyl)phosphine
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Tris(4-fluorophenyl)phosphine is widely used as a ligand in coordination chemistry and catalysis, particularly in transition metal-catalyzed reactions. Its electron-withdrawing fluorine substituents enhance the stability and reactivity of metal complexes, making it valuable in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. It also finds application in the synthesis of organic semiconductors and optoelectronic materials due to its ability to modify electronic properties. Additionally,

Tris(4-fluorophenyl)phosphine is widely used as a ligand in coordination chemistry and catalysis, particularly in transition metal-catalyzed reactions. Its electron-withdrawing fluorine substituents enhance the stability and reactivity of metal complexes, making it valuable in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. It also finds application in the synthesis of organic semiconductors and optoelectronic materials due to its ability to modify electronic properties. Additionally, it serves as a precursor in the preparation of phosphine-based polymers and advanced materials for use in sensors and coatings. Its role in asymmetric catalysis further highlights its importance in producing chiral compounds for pharmaceuticals and fine chemicals.

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