4-(DIMETHYLAMINO)PHENYLDIPHENYLPHOSPHINE

95.0%(GC)

Reagent Code: #68798
label
Alias 4-(Dimethylamino)phenyldiphenylphosphine
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CAS Number 739-58-2

science Other reagents with same CAS 739-58-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.35 g/mol
Formula C₂₀H₂₀NP
badge Registry Numbers
MDL Number MFCD00192068
thermostat Physical Properties
Melting Point 151-154 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is widely used as a ligand in coordination chemistry and catalysis. Its ability to form stable complexes with transition metals makes it valuable in various catalytic processes, such as cross-coupling reactions, hydrogenation, and carbonylation. It is particularly effective in palladium-catalyzed reactions, where it enhances the efficiency and selectivity of the catalyst. Additionally, it finds applications in organic synthesis, where it aids in the formation of carbon-phosphorus bonds. Its role in stabilizing metal complexes also makes it useful in the development of advanced materials and in the study of organometallic chemistry.

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Test Parameter Specification
Purity 95-100%
Appearance Off-white solid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿280.00
inventory 1g
10-20 days ฿350.00
inventory 5g
10-20 days ฿1,200.00

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4-(DIMETHYLAMINO)PHENYLDIPHENYLPHOSPHINE
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This chemical is widely used as a ligand in coordination chemistry and catalysis. Its ability to form stable complexes with transition metals makes it valuable in various catalytic processes, such as cross-coupling reactions, hydrogenation, and carbonylation. It is particularly effective in palladium-catalyzed reactions, where it enhances the efficiency and selectivity of the catalyst. Additionally, it finds applications in organic synthesis, where it aids in the formation of carbon-phosphorus bonds. Its

This chemical is widely used as a ligand in coordination chemistry and catalysis. Its ability to form stable complexes with transition metals makes it valuable in various catalytic processes, such as cross-coupling reactions, hydrogenation, and carbonylation. It is particularly effective in palladium-catalyzed reactions, where it enhances the efficiency and selectivity of the catalyst. Additionally, it finds applications in organic synthesis, where it aids in the formation of carbon-phosphorus bonds. Its role in stabilizing metal complexes also makes it useful in the development of advanced materials and in the study of organometallic chemistry.

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