N-Phenylpyrrol-2-yldi-tert-butylphosphine

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Reagent Code: #218581
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CAS Number 672937-61-0

science Other reagents with same CAS 672937-61-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.38 g/mol
Formula C₁₈H₂₆NP
badge Registry Numbers
MDL Number MFCD05861612
thermostat Physical Properties
Boiling Point 386.3 ℃ at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a ligand in palladium-catalyzed cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Its bulky di-tert-butylphosphine group enhances electron density on the metal center, improving catalytic activity and stability. The N-phenylpyrrole moiety contributes to solubility and can influence the steric environment around the metal, enabling selective transformations. Commonly applied in the synthesis of pharmaceuticals, agrochemicals, and functional materials where efficient C–C and C–N bond formation is required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,020.00

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N-Phenylpyrrol-2-yldi-tert-butylphosphine
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Used as a ligand in palladium-catalyzed cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Its bulky di-tert-butylphosphine group enhances electron density on the metal center, improving catalytic activity and stability. The N-phenylpyrrole moiety contributes to solubility and can influence the steric environment around the metal, enabling selective transformations. Commonly applied in the synthesis of pharmaceuticals, agrochemicals, and functional materials where e

Used as a ligand in palladium-catalyzed cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Its bulky di-tert-butylphosphine group enhances electron density on the metal center, improving catalytic activity and stability. The N-phenylpyrrole moiety contributes to solubility and can influence the steric environment around the metal, enabling selective transformations. Commonly applied in the synthesis of pharmaceuticals, agrochemicals, and functional materials where efficient C–C and C–N bond formation is required.

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