Tris(2-thienyl)phosphine

98%

Reagent Code: #68871
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Alias Tris(2-thienyl)phosphine
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CAS Number 24171-89-9

science Other reagents with same CAS 24171-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.371 g/mol
Formula C₁₂H₉PS₃
badge Registry Numbers
EC Number 246-059-8
MDL Number MFCD00015471
thermostat Physical Properties
Melting Point 29-30 °C
Boiling Point 205 °C / 2mmHg
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Tris(2-thienyl)phosphine is widely used in the field of organic synthesis, particularly as a ligand in transition metal catalysis. It plays a crucial role in facilitating various cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are essential for constructing complex organic molecules. Its electron-rich nature and steric properties make it effective in stabilizing metal centers and enhancing catalytic activity.

In material science, this compound is employed in the development of organic semiconductors and conductive polymers. Its incorporation into polymer matrices can improve charge transport properties, making it valuable for applications in organic electronics, including organic light-emitting diodes (OLEDs) and photovoltaic devices.

Additionally, Tris(2-thienyl)phosphine is utilized in coordination chemistry to synthesize metal complexes with unique optical and electronic properties. These complexes are often explored for their potential in catalysis, sensing, and luminescent materials. Its versatility and effectiveness in these applications highlight its importance in both academic research and industrial processes.

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Test Parameter Specification
Freezing Point 27-30
Purity (GC) 98-100%
Note Low melting point solid; may change state in different environments (solid, liquid, or semi-solid)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,431.00
inventory 5g
10-20 days ฿6,021.00
inventory 25g
10-20 days ฿25,200.00

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Tris(2-thienyl)phosphine
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Tris(2-thienyl)phosphine is widely used in the field of organic synthesis, particularly as a ligand in transition metal catalysis. It plays a crucial role in facilitating various cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are essential for constructing complex organic molecules. Its electron-rich nature and steric properties make it effective in stabilizing metal centers and enhancing catalytic activity.

In material science, this compound is employed in the developme

Tris(2-thienyl)phosphine is widely used in the field of organic synthesis, particularly as a ligand in transition metal catalysis. It plays a crucial role in facilitating various cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are essential for constructing complex organic molecules. Its electron-rich nature and steric properties make it effective in stabilizing metal centers and enhancing catalytic activity.

In material science, this compound is employed in the development of organic semiconductors and conductive polymers. Its incorporation into polymer matrices can improve charge transport properties, making it valuable for applications in organic electronics, including organic light-emitting diodes (OLEDs) and photovoltaic devices.

Additionally, Tris(2-thienyl)phosphine is utilized in coordination chemistry to synthesize metal complexes with unique optical and electronic properties. These complexes are often explored for their potential in catalysis, sensing, and luminescent materials. Its versatility and effectiveness in these applications highlight its importance in both academic research and industrial processes.

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