Tris[3,5-bis(trifluoromethyl)phenyl]phosphine

98.0%(GC)

Reagent Code: #68882
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Alias Tris[N,N-bis(trimethylsilyl)amine]phosphine; Tris[3,4-bis(trifluoromethyl)phenyl]phosphine
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CAS Number 175136-62-6

science Other reagents with same CAS 175136-62-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 670.27 g/mol
Formula C₂₄H₉F₁₈P
badge Registry Numbers
MDL Number MFCD00042428
thermostat Physical Properties
Melting Point 95 °C
Boiling Point 128-130°C 0,5mm
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used as a ligand in catalytic processes, especially in transition metal-catalyzed reactions. Its electron-deficient nature, due to the trifluoromethyl groups, makes it highly effective in stabilizing metal centers and enhancing the reactivity of catalysts. It is commonly employed in cross-coupling reactions, such as Suzuki and Heck couplings, where it improves yield and selectivity. Additionally, it finds application in asymmetric synthesis, where its steric bulk and electronic properties help control the stereochemistry of the reaction. It is also utilized in the synthesis of pharmaceuticals and fine chemicals, where precise catalytic activity is crucial. Its stability under harsh reaction conditions further broadens its utility in industrial and laboratory settings.

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Test Parameter Specification
Purity (GC) 98-100%
Appearance Yellow-brown

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,820.00
inventory 1g
10-20 days ฿6,240.00
inventory 50mg
10-20 days ฿850.00
inventory 5g
10-20 days ฿23,580.00

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Tris[3,5-bis(trifluoromethyl)phenyl]phosphine
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This chemical is primarily used as a ligand in catalytic processes, especially in transition metal-catalyzed reactions. Its electron-deficient nature, due to the trifluoromethyl groups, makes it highly effective in stabilizing metal centers and enhancing the reactivity of catalysts. It is commonly employed in cross-coupling reactions, such as Suzuki and Heck couplings, where it improves yield and selectivity. Additionally, it finds application in asymmetric synthesis, where its steric bulk and electronic

This chemical is primarily used as a ligand in catalytic processes, especially in transition metal-catalyzed reactions. Its electron-deficient nature, due to the trifluoromethyl groups, makes it highly effective in stabilizing metal centers and enhancing the reactivity of catalysts. It is commonly employed in cross-coupling reactions, such as Suzuki and Heck couplings, where it improves yield and selectivity. Additionally, it finds application in asymmetric synthesis, where its steric bulk and electronic properties help control the stereochemistry of the reaction. It is also utilized in the synthesis of pharmaceuticals and fine chemicals, where precise catalytic activity is crucial. Its stability under harsh reaction conditions further broadens its utility in industrial and laboratory settings.

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