Tris(2,4-dimethylphenyl)phosphine

97%

Reagent Code: #121809
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Alias Tris(2,4-xylyl)phosphine
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CAS Number 49676-42-8

science Other reagents with same CAS 49676-42-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 346.44 g/mol
Formula C₂₄H₂₇P
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MDL Number MFCD09039068
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Tris(2,4-dimethylphenyl)phosphine is primarily used as a ligand in coordination chemistry and catalysis. It plays a significant role in the synthesis of organometallic compounds, particularly in transition metal-catalyzed reactions. Its sterically hindered structure makes it effective in stabilizing metal complexes, enhancing selectivity and efficiency in processes such as cross-coupling reactions, hydrogenation, and polymerization. Additionally, it is utilized in the development of advanced materials, including phosphorescent compounds for organic light-emitting diodes (OLEDs). Its application extends to pharmaceutical research, where it aids in the creation of complex molecular structures through precise catalytic processes.

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Test Parameter Specification
Melting Point 158-162
Purity (HPLC) 97-100%
Appearance White to yellow powder
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿981.00
inventory 5g
10-20 days ฿3,897.00

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Tris(2,4-dimethylphenyl)phosphine
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Tris(2,4-dimethylphenyl)phosphine is primarily used as a ligand in coordination chemistry and catalysis. It plays a significant role in the synthesis of organometallic compounds, particularly in transition metal-catalyzed reactions. Its sterically hindered structure makes it effective in stabilizing metal complexes, enhancing selectivity and efficiency in processes such as cross-coupling reactions, hydrogenation, and polymerization. Additionally, it is utilized in the development of advanced materials, i

Tris(2,4-dimethylphenyl)phosphine is primarily used as a ligand in coordination chemistry and catalysis. It plays a significant role in the synthesis of organometallic compounds, particularly in transition metal-catalyzed reactions. Its sterically hindered structure makes it effective in stabilizing metal complexes, enhancing selectivity and efficiency in processes such as cross-coupling reactions, hydrogenation, and polymerization. Additionally, it is utilized in the development of advanced materials, including phosphorescent compounds for organic light-emitting diodes (OLEDs). Its application extends to pharmaceutical research, where it aids in the creation of complex molecular structures through precise catalytic processes.

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