1,3-Dibenzyl-4,5-dimethyl-1H-imidazol-3-ium chloride
95%
- Product Code: 167438
CAS:
596093-98-0
| Molecular Weight: | 312.84 g./mol | Molecular Formula: | C₁₉H₂₁N₂.Cl |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used as a precursor in the synthesis of N-heterocyclic carbene (NHC) ligands, this compound plays a key role in catalysis, particularly in organometallic reactions such as cross-coupling, olefin metathesis, and hydrogenation. The imidazolium core stabilizes metal centers when deprotonated, forming robust NHC-metal complexes that exhibit high thermal stability and catalytic efficiency. It is especially valued in research settings for developing new catalysts with improved activity and selectivity. Additionally, its benzyl and methyl substituents influence solubility and steric properties, making it suitable for fine-tuning catalyst performance in both academic and industrial applications.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 10mg | 10-20 days | ฿16,970.00 |
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| 25mg | 10-20 days | ฿32,250.00 |
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| 50mg | 10-20 days | ฿54,810.00 |
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1,3-Dibenzyl-4,5-dimethyl-1H-imidazol-3-ium chloride
Used as a precursor in the synthesis of N-heterocyclic carbene (NHC) ligands, this compound plays a key role in catalysis, particularly in organometallic reactions such as cross-coupling, olefin metathesis, and hydrogenation. The imidazolium core stabilizes metal centers when deprotonated, forming robust NHC-metal complexes that exhibit high thermal stability and catalytic efficiency. It is especially valued in research settings for developing new catalysts with improved activity and selectivity. Additionally, its benzyl and methyl substituents influence solubility and steric properties, making it suitable for fine-tuning catalyst performance in both academic and industrial applications.
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