Chloro[(1,2,3-h)-3-phenyl-2-propenyl][1,3-bis(2,6-diisopropylphenyl)-4,5-di-H-imidazol-2-ylidene]palladium(II)

98%

Reagent Code: #162627
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CAS Number 884879-24-7

science Other reagents with same CAS 884879-24-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 649.64 g/mol
Formula C₃₆H₄₇ClN₂Pd
badge Registry Numbers
MDL Number MFCD09265339
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Widely used as a highly active catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Heck reactions, enabling efficient carbon-carbon bond formation. Its robust structure enhances catalytic efficiency and stability under various reaction conditions, making it suitable for synthesizing complex organic molecules, including pharmaceuticals and fine chemicals. The presence of bulky N-heterocyclic carbene ligand improves catalyst longevity and turnover, even at low loading levels. Commonly applied in industrial and academic research settings for streamlining synthetic routes and improving yields in heterocycle and biaryl synthesis.

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Test Parameter Specification
Appearance Light yellow to yellow to orange powder
Purity (%) 97.5-100%
Palladium (Pd) 16.0-17.0%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,160.00
inventory 1g
10-20 days ฿9,230.00
inventory 100mg
10-20 days ฿2,380.00

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Chloro[(1,2,3-h)-3-phenyl-2-propenyl][1,3-bis(2,6-diisopropylphenyl)-4,5-di-H-imidazol-2-ylidene]palladium(II)
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Widely used as a highly active catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Heck reactions, enabling efficient carbon-carbon bond formation. Its robust structure enhances catalytic efficiency and stability under various reaction conditions, making it suitable for synthesizing complex organic molecules, including pharmaceuticals and fine chemicals. The presence of bulky N-heterocyclic carbene ligand improves catalyst longevity and turnover, even at low loading levels. Commonly applied in industrial and academic research settings for streamlining synthetic routes and improving yields in heterocycle and biaryl synthesis.
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