(T-4)-Dichloro(2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-N1,N10)-Nickel

98%

Reagent Code: #238954
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CAS Number 120763-13-5

science Other reagents with same CAS 120763-13-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 490.05 g/mol
Formula C₂₆H₂₀Cl₂N₂Ni
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It facilitates reactions such as Negishi and Suzuki couplings, where its stability and electron-deficient nature enhance catalytic efficiency. The ligand structure provides steric bulk and electronic tuning, improving selectivity and yield in organic synthesis. Commonly applied in the preparation of pharmaceuticals, agrochemicals, and fine chemicals where precise bond formation is critical. Also employed in materials science for synthesizing conjugated polymers and organic electronic materials due to its reliable performance under mild reaction conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,460.00
inventory 1g
10-20 days ฿15,840.00
inventory 250mg
10-20 days ฿5,870.00
(T-4)-Dichloro(2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-N1,N10)-Nickel
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Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It facilitates reactions such as Negishi and Suzuki couplings, where its stability and electron-deficient nature enhance catalytic efficiency. The ligand structure provides steric bulk and electronic tuning, improving selectivity and yield in organic synthesis. Commonly applied in the preparation of pharmaceuticals, agrochemicals, and fine chemicals where precise bond formation is critical. Also employed

Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It facilitates reactions such as Negishi and Suzuki couplings, where its stability and electron-deficient nature enhance catalytic efficiency. The ligand structure provides steric bulk and electronic tuning, improving selectivity and yield in organic synthesis. Commonly applied in the preparation of pharmaceuticals, agrochemicals, and fine chemicals where precise bond formation is critical. Also employed in materials science for synthesizing conjugated polymers and organic electronic materials due to its reliable performance under mild reaction conditions.

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