N-(2-Methoxyphenyl)-2-(di-t-butylphosphino)pyrrole

≥95%

Reagent Code: #219688
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CAS Number 1053658-91-5

science Other reagents with same CAS 1053658-91-5

blur_circular Chemical Specifications

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Weight 317.41 g/mol
Formula C₁₉H₂₈NOP
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MDL Number MFCD06798301
inventory_2 Storage & Handling
Storage Room temperature, argon

description Product Description

Used as a specialized ligand in palladium-catalyzed cross-coupling reactions, particularly in Buchwald–Hartwig amination, enabling efficient carbon–nitrogen bond formation. Its steric bulk and electron-rich phosphine group enhance catalyst stability and reactivity, allowing reactions to proceed under milder conditions with high selectivity. Commonly applied in the synthesis of pharmaceuticals, agrochemicals, and functional materials where precise C–N coupling is required. Also employed in the preparation of complex organic molecules, including heterocycles and natural product derivatives, due to its compatibility with a wide range of substrates and functional groups.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿16,000.00

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N-(2-Methoxyphenyl)-2-(di-t-butylphosphino)pyrrole
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Used as a specialized ligand in palladium-catalyzed cross-coupling reactions, particularly in Buchwald–Hartwig amination, enabling efficient carbon–nitrogen bond formation. Its steric bulk and electron-rich phosphine group enhance catalyst stability and reactivity, allowing reactions to proceed under milder conditions with high selectivity. Commonly applied in the synthesis of pharmaceuticals, agrochemicals, and functional materials where precise C–N coupling is required. Also employed in the preparation

Used as a specialized ligand in palladium-catalyzed cross-coupling reactions, particularly in Buchwald–Hartwig amination, enabling efficient carbon–nitrogen bond formation. Its steric bulk and electron-rich phosphine group enhance catalyst stability and reactivity, allowing reactions to proceed under milder conditions with high selectivity. Commonly applied in the synthesis of pharmaceuticals, agrochemicals, and functional materials where precise C–N coupling is required. Also employed in the preparation of complex organic molecules, including heterocycles and natural product derivatives, due to its compatibility with a wide range of substrates and functional groups.

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