Tris(3-chlorophenyl)phosphine

98%

Reagent Code: #121798
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Alias Tris(3-chlorophenyl)phosphine
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CAS Number 29949-85-7

science Other reagents with same CAS 29949-85-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 365.63 g/mol
Formula C₁₈H₁₂Cl₃P
badge Registry Numbers
EC Number 214-596-7
MDL Number MFCD00013639
thermostat Physical Properties
Melting Point 64-66°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Tris(3-chlorophenyl)phosphine is primarily used as a ligand in coordination chemistry, particularly in the synthesis of metal complexes. It plays a significant role in catalysis, especially in palladium-catalyzed cross-coupling reactions such as Suzuki and Heck reactions, which are essential in the production of pharmaceuticals and fine chemicals. Its electron-withdrawing chlorine substituents enhance the stability and reactivity of the resulting metal complexes, making it valuable in organic synthesis. Additionally, it finds application in materials science, where it is used to modify the properties of polymers and other advanced materials.

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Test Parameter Specification
Purity (%) 98-100%
Phosphorus NMR Spectra Conforms To Structure
Proton NMR Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿18,320.00
inventory 1g
10-20 days ฿3,760.00

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Tris(3-chlorophenyl)phosphine
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Tris(3-chlorophenyl)phosphine is primarily used as a ligand in coordination chemistry, particularly in the synthesis of metal complexes. It plays a significant role in catalysis, especially in palladium-catalyzed cross-coupling reactions such as Suzuki and Heck reactions, which are essential in the production of pharmaceuticals and fine chemicals. Its electron-withdrawing chlorine substituents enhance the stability and reactivity of the resulting metal complexes, making it valuable in organic synthesis.

Tris(3-chlorophenyl)phosphine is primarily used as a ligand in coordination chemistry, particularly in the synthesis of metal complexes. It plays a significant role in catalysis, especially in palladium-catalyzed cross-coupling reactions such as Suzuki and Heck reactions, which are essential in the production of pharmaceuticals and fine chemicals. Its electron-withdrawing chlorine substituents enhance the stability and reactivity of the resulting metal complexes, making it valuable in organic synthesis. Additionally, it finds application in materials science, where it is used to modify the properties of polymers and other advanced materials.

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