Dichlorobis(isoquinoline)-Palladium

98%

Reagent Code: #178525
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CAS Number 23807-51-4

science Other reagents with same CAS 23807-51-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 435.64 g/mol
Formula C₁₈H₁₄Cl₂N₂Pd
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Widely used as a catalyst in cross-coupling reactions, particularly in organic synthesis for forming carbon-carbon bonds. It enables reactions such as Suzuki, Heck, and Negishi couplings, which are essential in pharmaceutical and agrochemical industries for constructing complex molecules. Its stability and reactivity make it suitable for catalyzing transformations under mild conditions, often with high selectivity and yield. Commonly employed in the synthesis of biaryl compounds, conjugated systems, and functionalized heterocycles used in drug development and materials science.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿9,700.00
250mg
10-20 days ฿14,500.00
1g
10-20 days ฿36,210.00
5g
10-20 days ฿134,790.00
Dichlorobis(isoquinoline)-Palladium
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Widely used as a catalyst in cross-coupling reactions, particularly in organic synthesis for forming carbon-carbon bonds. It enables reactions such as Suzuki, Heck, and Negishi couplings, which are essential in pharmaceutical and agrochemical industries for constructing complex molecules. Its stability and reactivity make it suitable for catalyzing transformations under mild conditions, often with high selectivity and yield. Commonly employed in the synthesis of biaryl compounds, conjugated systems, and

Widely used as a catalyst in cross-coupling reactions, particularly in organic synthesis for forming carbon-carbon bonds. It enables reactions such as Suzuki, Heck, and Negishi couplings, which are essential in pharmaceutical and agrochemical industries for constructing complex molecules. Its stability and reactivity make it suitable for catalyzing transformations under mild conditions, often with high selectivity and yield. Commonly employed in the synthesis of biaryl compounds, conjugated systems, and functionalized heterocycles used in drug development and materials science.

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