Dibromobis(triphenylphosphine)nickel(II)

99%

Reagent Code: #169228
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Alias Nickel dibromoblast (triphenylphosphorus)
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CAS Number 14126-37-5

science Other reagents with same CAS 14126-37-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 743.07 g/mol
Formula C₃₆H₃₀Br₂NiP₂
badge Registry Numbers
MDL Number MFCD00015865
thermostat Physical Properties
Melting Point 219-223 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8 ℃, dry, inert gas atmosphere

description Product Description

Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It plays a key role in Ullmann-type reactions and other nickel-catalyzed coupling processes, offering an alternative to palladium-based systems. Its stability and reactivity make it suitable for transformations in organic synthesis, including aryl-aryl and aryl-heteroaryl bond formations. Commonly applied in the development of pharmaceuticals, agrochemicals, and advanced materials where efficient and selective coupling is required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿180.00
5g
10-20 days ฿440.00
25g
10-20 days ฿1,320.00
100g
10-20 days ฿5,080.00
500g
10-20 days ฿20,500.00
Dibromobis(triphenylphosphine)nickel(II)
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Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It plays a key role in Ullmann-type reactions and other nickel-catalyzed coupling processes, offering an alternative to palladium-based systems. Its stability and reactivity make it suitable for transformations in organic synthesis, including aryl-aryl and aryl-heteroaryl bond formations. Commonly applied in the development of pharmaceuticals, agrochemicals, and advanced materials where efficient and sel

Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It plays a key role in Ullmann-type reactions and other nickel-catalyzed coupling processes, offering an alternative to palladium-based systems. Its stability and reactivity make it suitable for transformations in organic synthesis, including aryl-aryl and aryl-heteroaryl bond formations. Commonly applied in the development of pharmaceuticals, agrochemicals, and advanced materials where efficient and selective coupling is required.

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