2-(Di(adamantan-1-yl)phosphino)-N,N-dimethylaniline

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Reagent Code: #68739
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CAS Number 1219080-77-9

science Other reagents with same CAS 1219080-77-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 421.6 g/mol
Formula C₂₈H₄NP
badge Registry Numbers
MDL Number MFCD17018758
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal catalysis. Its unique structure, featuring adamantyl groups, enhances steric bulk and electron-donating properties, making it effective in facilitating challenging chemical transformations. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it improves reaction efficiency and selectivity. Additionally, its stability and robustness make it suitable for use in harsh reaction conditions, including high temperatures and strong bases. The compound is also explored in the development of new pharmaceuticals and fine chemicals, where precise control over reaction pathways is crucial.

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Test Parameter Specification
Appearance White to Off-White to Yellow Powder or Crystals
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,384.00
inventory 250mg
10-20 days ฿4,923.00

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2-(Di(adamantan-1-yl)phosphino)-N,N-dimethylaniline
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This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal catalysis. Its unique structure, featuring adamantyl groups, enhances steric bulk and electron-donating properties, making it effective in facilitating challenging chemical transformations. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it improves reaction efficiency and selectivity. Additionally, its stability and robustness make it sui

This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal catalysis. Its unique structure, featuring adamantyl groups, enhances steric bulk and electron-donating properties, making it effective in facilitating challenging chemical transformations. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it improves reaction efficiency and selectivity. Additionally, its stability and robustness make it suitable for use in harsh reaction conditions, including high temperatures and strong bases. The compound is also explored in the development of new pharmaceuticals and fine chemicals, where precise control over reaction pathways is crucial.

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