Tris(4-chlorophenyl)phosphine

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Reagent Code: #121799
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CAS Number 1159-54-2

science Other reagents with same CAS 1159-54-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 365.62 g/mol
Formula ClC₆H₄₃P
badge Registry Numbers
EC Number 214-596-7
MDL Number MFCD00013639
thermostat Physical Properties
Melting Point 100-103 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Tris(4-chlorophenyl)phosphine is primarily used as a ligand in coordination chemistry and catalysis. It is often employed in the synthesis of organometallic compounds, where it facilitates various transition metal-catalyzed reactions, such as cross-coupling reactions, hydrogenation, and hydroformylation. Its electron-withdrawing chlorophenyl groups enhance the stability and reactivity of the metal complexes it forms, making it valuable in creating efficient catalytic systems. Additionally, it finds applications in the development of phosphorescent materials and organic light-emitting diodes (OLEDs), where it contributes to the tuning of electronic properties. In research, it is utilized as a reagent for studying phosphine-based chemistry and designing novel catalysts for organic transformations.

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Test Parameter Specification
Melting Point 102-103
Purity (GC) 98-100%
31P NMR Spectrum Conforms To Structure
Appearance White to light yellow flakes, crystals, or powder
Infrared Spectrum Conforms To Structure
NMR (1H-NMR) Complies

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿5,560.00
inventory 100g
10-20 days ฿19,620.00
inventory 5g
10-20 days ฿2,420.00
inventory 1g
10-20 days ฿680.00

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Tris(4-chlorophenyl)phosphine
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Tris(4-chlorophenyl)phosphine is primarily used as a ligand in coordination chemistry and catalysis. It is often employed in the synthesis of organometallic compounds, where it facilitates various transition metal-catalyzed reactions, such as cross-coupling reactions, hydrogenation, and hydroformylation. Its electron-withdrawing chlorophenyl groups enhance the stability and reactivity of the metal complexes it forms, making it valuable in creating efficient catalytic systems. Additionally, it finds appli

Tris(4-chlorophenyl)phosphine is primarily used as a ligand in coordination chemistry and catalysis. It is often employed in the synthesis of organometallic compounds, where it facilitates various transition metal-catalyzed reactions, such as cross-coupling reactions, hydrogenation, and hydroformylation. Its electron-withdrawing chlorophenyl groups enhance the stability and reactivity of the metal complexes it forms, making it valuable in creating efficient catalytic systems. Additionally, it finds applications in the development of phosphorescent materials and organic light-emitting diodes (OLEDs), where it contributes to the tuning of electronic properties. In research, it is utilized as a reagent for studying phosphine-based chemistry and designing novel catalysts for organic transformations.

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