Chloro(1,5-cyclooctadiene)methylpalladium(II)

98%

Reagent Code: #162624
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CAS Number 63936-85-6

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.0487 g/mol
Formula C₉H₁₀ClPd
badge Registry Numbers
MDL Number MFCD16621448
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Widely used as a catalyst precursor in homogeneous catalysis, especially in cross-coupling reactions such as Mizoroki-Heck, Suzuki-Miyaura, and Sonogashira couplings. It facilitates carbon-carbon bond formation under mild conditions due to the labile cyclooctadiene ligand, which allows for easy generation of active palladium species. Commonly employed in organic synthesis for pharmaceuticals, agrochemicals, and fine chemicals. Its solubility in organic solvents and moderate stability make it convenient for use in air-sensitive reactions when handled under inert atmosphere. Also serves as a starting material for synthesizing other palladium catalysts with tailored ligands.

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Test Parameter Specification
Appearance White to light brown solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure
ICP: Confirms Pd Component Confirmed

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,800.00
inventory 1g
10-20 days ฿6,600.00
inventory 100mg
10-20 days ฿750.00

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Chloro(1,5-cyclooctadiene)methylpalladium(II)
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Widely used as a catalyst precursor in homogeneous catalysis, especially in cross-coupling reactions such as Mizoroki-Heck, Suzuki-Miyaura, and Sonogashira couplings. It facilitates carbon-carbon bond formation under mild conditions due to the labile cyclooctadiene ligand, which allows for easy generation of active palladium species. Commonly employed in organic synthesis for pharmaceuticals, agrochemicals, and fine chemicals. Its solubility in organic solvents and moderate stability make it convenient f

Widely used as a catalyst precursor in homogeneous catalysis, especially in cross-coupling reactions such as Mizoroki-Heck, Suzuki-Miyaura, and Sonogashira couplings. It facilitates carbon-carbon bond formation under mild conditions due to the labile cyclooctadiene ligand, which allows for easy generation of active palladium species. Commonly employed in organic synthesis for pharmaceuticals, agrochemicals, and fine chemicals. Its solubility in organic solvents and moderate stability make it convenient for use in air-sensitive reactions when handled under inert atmosphere. Also serves as a starting material for synthesizing other palladium catalysts with tailored ligands.

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