1-(2,6-Diisopropylphenyl)-3-mesityl-4,5-dihydro-1H-imidazol-3-ium chloride

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Reagent Code: #70570
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CAS Number 866926-59-2

science Other reagents with same CAS 866926-59-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 384.9852 g/mol
Formula C₂₄H₃₃ClN₂
badge Registry Numbers
MDL Number MFCD08276860
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily used as a precursor or intermediate in the synthesis of N-heterocyclic carbenes (NHCs), which are valuable ligands in organometallic chemistry. These ligands are widely employed in catalysis, particularly in transition metal-catalyzed reactions such as cross-coupling, hydrogenation, and polymerization processes. Its sterically bulky structure enhances the stability and reactivity of the resulting metal complexes, making it suitable for applications in fine chemical synthesis and industrial-scale catalytic processes. Additionally, it may be utilized in the development of ionic liquids or as a stabilizer in certain chemical reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,160.00
inventory 1g
10-20 days ฿5,922.00

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1-(2,6-Diisopropylphenyl)-3-mesityl-4,5-dihydro-1H-imidazol-3-ium chloride
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This chemical is primarily used as a precursor or intermediate in the synthesis of N-heterocyclic carbenes (NHCs), which are valuable ligands in organometallic chemistry. These ligands are widely employed in catalysis, particularly in transition metal-catalyzed reactions such as cross-coupling, hydrogenation, and polymerization processes. Its sterically bulky structure enhances the stability and reactivity of the resulting metal complexes, making it suitable for applications in fine chemical synthesis an

This chemical is primarily used as a precursor or intermediate in the synthesis of N-heterocyclic carbenes (NHCs), which are valuable ligands in organometallic chemistry. These ligands are widely employed in catalysis, particularly in transition metal-catalyzed reactions such as cross-coupling, hydrogenation, and polymerization processes. Its sterically bulky structure enhances the stability and reactivity of the resulting metal complexes, making it suitable for applications in fine chemical synthesis and industrial-scale catalytic processes. Additionally, it may be utilized in the development of ionic liquids or as a stabilizer in certain chemical reactions.

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