Dichloro(4,4'-dimethoxy-2,2'-bipyridine-κN1,κN1')-Nickel

95%

Reagent Code: #215718
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CAS Number 1303613-81-1

science Other reagents with same CAS 1303613-81-1

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Weight 345.84 g/mol
Formula C₁₂H₁₂Cl₂N₂NiO₂
badge Registry Numbers
MDL Number MFCD32672287
inventory_2 Storage & Handling
Storage Room temperature, light-proof, 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 Kumada and Negishi couplings, which are essential in synthesizing complex organic molecules for pharmaceuticals, agrochemicals, and advanced materials. The presence of the dimethoxy-substituted bipyridine ligand enhances stability and electron donation, improving catalytic efficiency and selectivity under mild conditions. Also employed in research for developing nickel-based catalytic systems as a more economical alternative to palladium catalysts.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,520.00
inventory 1g
10-20 days ฿7,170.00
inventory 5g
10-20 days ฿25,030.00

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Dichloro(4,4'-dimethoxy-2,2'-bipyridine-κN1,κN1')-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 Kumada and Negishi couplings, which are essential in synthesizing complex organic molecules for pharmaceuticals, agrochemicals, and advanced materials. The presence of the dimethoxy-substituted bipyridine ligand enhances stability and electron donation, improving catalytic efficiency and selectivity under mild conditions. Also employed in research for developing nickel-based
Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It facilitates reactions such as Kumada and Negishi couplings, which are essential in synthesizing complex organic molecules for pharmaceuticals, agrochemicals, and advanced materials. The presence of the dimethoxy-substituted bipyridine ligand enhances stability and electron donation, improving catalytic efficiency and selectivity under mild conditions. Also employed in research for developing nickel-based catalytic systems as a more economical alternative to palladium catalysts.
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