1,6-Bis(diphenylphosphino)hexane

97%

Reagent Code: #68735
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Alias 1,6-bis(diphenylphosphino)hexane; 1,6-bisdiphenylphosphinohexane
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CAS Number 19845-69-3

science Other reagents with same CAS 19845-69-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 454.52 g/mol
Formula C₃₀H₃₂P₂
badge Registry Numbers
MDL Number MFCD00003053
thermostat Physical Properties
Melting Point 124-126 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

1,6-Bis(diphenylphosphino)hexane is primarily used as a ligand in coordination chemistry and catalysis. It forms stable complexes with transition metals, such as palladium, platinum, and nickel, which are essential in various catalytic processes. These metal complexes are often employed in cross-coupling reactions, including Suzuki and Heck reactions, which are widely used in organic synthesis to form carbon-carbon bonds. Additionally, its bidentate nature allows for effective chelation, enhancing the stability and reactivity of the metal centers in catalytic systems. This compound is also utilized in the development of advanced materials and in research focused on understanding the mechanisms of catalytic reactions.

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Test Parameter Specification
Melting Point 124-128
Purity 97-100
Appearance White to light yellow powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿9,980.00
inventory 25g
10-20 days ฿2,900.00
inventory 1g
10-20 days ฿290.00
inventory 5g
10-20 days ฿660.00

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1,6-Bis(diphenylphosphino)hexane
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1,6-Bis(diphenylphosphino)hexane is primarily used as a ligand in coordination chemistry and catalysis. It forms stable complexes with transition metals, such as palladium, platinum, and nickel, which are essential in various catalytic processes. These metal complexes are often employed in cross-coupling reactions, including Suzuki and Heck reactions, which are widely used in organic synthesis to form carbon-carbon bonds. Additionally, its bidentate nature allows for effective chelation, enhancing the stability and reactivity of the metal centers in catalytic systems. This compound is also utilized in the development of advanced materials and in research focused on understanding the mechanisms of catalytic reactions.
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