1,3-Di-t-butylbenzimidazolium chloride

97%

Reagent Code: #176543
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CAS Number 946607-10-9

science Other reagents with same CAS 946607-10-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.81 g/mol
Formula C₁₅H₂₃ClN₂
badge Registry Numbers
MDL Number MFCD08705247
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a precursor for generating N-heterocyclic carbenes (NHCs), particularly in catalytic applications. Its bulky t-butyl groups enhance steric protection, making the derived carbene suitable for stabilizing reactive metal centers in homogeneous catalysis. Commonly employed in palladium-catalyzed cross-coupling reactions, such as Suzuki and Heck reactions, where it improves catalyst longevity and activity. Also utilized in organocatalysis for promoting carbon–carbon and carbon–heteroatom bond formations. The chloride counterion facilitates easy salt metathesis, allowing incorporation into various catalytic systems.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿4,070.00
1g
10-20 days ฿13,610.00
5g
10-20 days ฿33,390.00
1,3-Di-t-butylbenzimidazolium chloride
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Used as a precursor for generating N-heterocyclic carbenes (NHCs), particularly in catalytic applications. Its bulky t-butyl groups enhance steric protection, making the derived carbene suitable for stabilizing reactive metal centers in homogeneous catalysis. Commonly employed in palladium-catalyzed cross-coupling reactions, such as Suzuki and Heck reactions, where it improves catalyst longevity and activity. Also utilized in organocatalysis for promoting carbon–carbon and carbon–heteroatom bond formatio

Used as a precursor for generating N-heterocyclic carbenes (NHCs), particularly in catalytic applications. Its bulky t-butyl groups enhance steric protection, making the derived carbene suitable for stabilizing reactive metal centers in homogeneous catalysis. Commonly employed in palladium-catalyzed cross-coupling reactions, such as Suzuki and Heck reactions, where it improves catalyst longevity and activity. Also utilized in organocatalysis for promoting carbon–carbon and carbon–heteroatom bond formations. The chloride counterion facilitates easy salt metathesis, allowing incorporation into various catalytic systems.

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