(SP-4-1)-[1, 3-Bis[2, 6-bis(1-ethylpropyl)phenyl]-4, 5-dichloro-1, 3-dihydro-2H-imidazol-2-ylidene]dichloro(3-chloropyridine-κN)palladium

98%

Reagent Code: #236483
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CAS Number 1435347-24-2

science Other reagents with same CAS 1435347-24-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 860.56 g/mol
Formula C₄₀H₅₄Cl₅N₃Pd
inventory_2 Storage & Handling
Storage 2-8°C, dry, light-proof

description Product Description

Widely used as a highly efficient catalyst in cross-coupling reactions, particularly in Buchwald–Hartwig amination and Suzuki–Miyaura coupling. Its robust structure allows for excellent activity with aryl chlorides, which are typically less reactive, enabling cost-effective and scalable synthesis of complex molecules. Commonly applied in pharmaceutical manufacturing for forming carbon–nitrogen and carbon–carbon bonds under mild conditions. Exhibits high thermal stability and prolonged catalyst lifetime, making it suitable for demanding industrial processes. Also employed in the synthesis of agrochemicals, functional materials, and fine chemicals where selectivity and yield are critical.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿7,240.00
100mg
10-20 days ฿13,120.00
250mg
10-20 days ฿22,710.00

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(SP-4-1)-[1, 3-Bis[2, 6-bis(1-ethylpropyl)phenyl]-4, 5-dichloro-1, 3-dihydro-2H-imidazol-2-ylidene]dichloro(3-chloropyridine-κN)palladium
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Widely used as a highly efficient catalyst in cross-coupling reactions, particularly in Buchwald–Hartwig amination and Suzuki–Miyaura coupling. Its robust structure allows for excellent activity with aryl chlorides, which are typically less reactive, enabling cost-effective and scalable synthesis of complex molecules. Commonly applied in pharmaceutical manufacturing for forming carbon–nitrogen and carbon–carbon bonds under mild conditions. Exhibits high thermal stability and prolonged catalyst lifetime,

Widely used as a highly efficient catalyst in cross-coupling reactions, particularly in Buchwald–Hartwig amination and Suzuki–Miyaura coupling. Its robust structure allows for excellent activity with aryl chlorides, which are typically less reactive, enabling cost-effective and scalable synthesis of complex molecules. Commonly applied in pharmaceutical manufacturing for forming carbon–nitrogen and carbon–carbon bonds under mild conditions. Exhibits high thermal stability and prolonged catalyst lifetime, making it suitable for demanding industrial processes. Also employed in the synthesis of agrochemicals, functional materials, and fine chemicals where selectivity and yield are critical.

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