Terakis(triphenylphosphine)palladium(0)

99.9% metals basis

Reagent Code: #239517
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CAS Number 14221-01-3

science Other reagents with same CAS 14221-01-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1155.56 g/mol
Formula C₇₂H₆₀P₄Pd
badge Registry Numbers
EC Number 238-086-9
MDL Number MFCD00010012
thermostat Physical Properties
Melting Point 103-107 °C
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Widely used as a catalyst in cross-coupling reactions, especially in organic synthesis and pharmaceutical manufacturing. It enables the formation of carbon-carbon bonds through reactions such as Suzuki, Heck, and Stille couplings. Its high activity and selectivity make it ideal for constructing complex molecules under mild conditions. Commonly employed in the synthesis of fine chemicals, agrochemicals, and advanced materials. The compound is particularly valued for its ability to facilitate coupling reactions with aryl and vinyl halides. Often used in research and industrial labs where efficient and reliable palladium-catalyzed transformations are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,230.00
inventory 1g
10-20 days ฿10,290.00
inventory 5g
10-20 days ฿20,590.00

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Terakis(triphenylphosphine)palladium(0)
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Widely used as a catalyst in cross-coupling reactions, especially in organic synthesis and pharmaceutical manufacturing. It enables the formation of carbon-carbon bonds through reactions such as Suzuki, Heck, and Stille couplings. Its high activity and selectivity make it ideal for constructing complex molecules under mild conditions. Commonly employed in the synthesis of fine chemicals, agrochemicals, and advanced materials. The compound is particularly valued for its ability to facilitate coupling reac

Widely used as a catalyst in cross-coupling reactions, especially in organic synthesis and pharmaceutical manufacturing. It enables the formation of carbon-carbon bonds through reactions such as Suzuki, Heck, and Stille couplings. Its high activity and selectivity make it ideal for constructing complex molecules under mild conditions. Commonly employed in the synthesis of fine chemicals, agrochemicals, and advanced materials. The compound is particularly valued for its ability to facilitate coupling reactions with aryl and vinyl halides. Often used in research and industrial labs where efficient and reliable palladium-catalyzed transformations are required.

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