Di(1-adamantyl)-n-butylphosphine hydriodide

98%

Reagent Code: #68960
label
Alias 2-(Diisopropylphosphine)ethylamine; n-Butyl-bis(1-adamantyl)phosphine; n-butylbis(1-adamantyl)phosphine hydroiodide;
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CAS Number 714951-87-8

science Other reagents with same CAS 714951-87-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.22 g/mol
Formula C₈H₂₀NP
badge Registry Numbers
MDL Number MFCD11044863
inventory_2 Storage & Handling
Storage Room temperature, inert gas protection

description Product Description

This compound is primarily utilized in organic synthesis, particularly as a ligand in transition metal catalysis. Its bulky structure enhances steric hindrance, making it effective in controlling the selectivity and reactivity of catalytic processes. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it aids in forming carbon-carbon bonds with high efficiency. Additionally, its stability under harsh reaction conditions makes it suitable for use in high-temperature or high-pressure environments. The compound is also explored in the development of advanced materials and pharmaceuticals, where precise control over molecular interactions is crucial.

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Test Parameter Specification
Purity 97.5-100%
Appearance White to light yellow powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,840.00
inventory 25g
10-20 days ฿19,490.00
inventory 250mg
10-20 days ฿590.00
inventory 5g
10-20 days ฿4,940.00

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Di(1-adamantyl)-n-butylphosphine hydriodide
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This compound is primarily utilized in organic synthesis, particularly as a ligand in transition metal catalysis. Its bulky structure enhances steric hindrance, making it effective in controlling the selectivity and reactivity of catalytic processes. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it aids in forming carbon-carbon bonds with high efficiency. Additionally, its stability under harsh reaction conditions makes it suitable for use in high-temp

This compound is primarily utilized in organic synthesis, particularly as a ligand in transition metal catalysis. Its bulky structure enhances steric hindrance, making it effective in controlling the selectivity and reactivity of catalytic processes. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it aids in forming carbon-carbon bonds with high efficiency. Additionally, its stability under harsh reaction conditions makes it suitable for use in high-temperature or high-pressure environments. The compound is also explored in the development of advanced materials and pharmaceuticals, where precise control over molecular interactions is crucial.

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