Chloro[(1,3-dimesitylimidazol-2-ylidene)(N,N-dimethylbenzylamine)palladium(II)]

98%

Reagent Code: #161277
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CAS Number 1058661-78-1

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Weight 580.51 g/mol
Formula C₃₀H₃₆ClN₃Pd
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Widely used as a highly active catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Heck reactions, enabling efficient carbon-carbon bond formation. Its robust structure enhances stability and turnover, making it suitable for coupling aryl chlorides, which are less reactive and more cost-effective substrates. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where high catalytic efficiency and functional group tolerance are required. Performs well under mild conditions and often allows for low catalyst loadings, reducing metal contamination in final products.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,980.00
inventory 1g
10-20 days ฿7,980.00
inventory 5g
10-20 days ฿29,980.00

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Chloro[(1,3-dimesitylimidazol-2-ylidene)(N,N-dimethylbenzylamine)palladium(II)]
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Widely used as a highly active catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Heck reactions, enabling efficient carbon-carbon bond formation. Its robust structure enhances stability and turnover, making it suitable for coupling aryl chlorides, which are less reactive and more cost-effective substrates. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where high catalytic efficiency and functional group tolerance are required. Performs well under mild

Widely used as a highly active catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Heck reactions, enabling efficient carbon-carbon bond formation. Its robust structure enhances stability and turnover, making it suitable for coupling aryl chlorides, which are less reactive and more cost-effective substrates. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where high catalytic efficiency and functional group tolerance are required. Performs well under mild conditions and often allows for low catalyst loadings, reducing metal contamination in final products.

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