(1,3-Bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene)copper(III)chloride

95%

Reagent Code: #155880
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CAS Number 915395-52-7

science Other reagents with same CAS 915395-52-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 489.611 g/mol
Formula C₂₇H₃₈ClCuN₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a highly efficient catalyst in cross-coupling reactions, particularly in carbon–carbon and carbon–heteroatom bond formations. It demonstrates high stability and reactivity under mild reaction conditions, making it suitable for synthesizing complex organic molecules in pharmaceutical and agrochemical industries. Its robust structure allows for excellent selectivity and yield in transformations such as arylation and alkylation, even with challenging substrates. Often preferred in reactions where traditional copper or palladium catalysts show limited efficiency or require harsher conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,710.00
inventory 1g
10-20 days ฿19,810.00
inventory 250mg
10-20 days ฿6,140.00

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(1,3-Bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene)copper(III)chloride
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Used as a highly efficient catalyst in cross-coupling reactions, particularly in carbon–carbon and carbon–heteroatom bond formations. It demonstrates high stability and reactivity under mild reaction conditions, making it suitable for synthesizing complex organic molecules in pharmaceutical and agrochemical industries. Its robust structure allows for excellent selectivity and yield in transformations such as arylation and alkylation, even with challenging substrates. Often preferred in reactions where tr

Used as a highly efficient catalyst in cross-coupling reactions, particularly in carbon–carbon and carbon–heteroatom bond formations. It demonstrates high stability and reactivity under mild reaction conditions, making it suitable for synthesizing complex organic molecules in pharmaceutical and agrochemical industries. Its robust structure allows for excellent selectivity and yield in transformations such as arylation and alkylation, even with challenging substrates. Often preferred in reactions where traditional copper or palladium catalysts show limited efficiency or require harsher conditions.

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