1-Cyclopentyl-3-mesityl-1H-imidazol-3-ium chloride
97%
- Product Code: 164154
CAS:
1583244-01-2
| Molecular Weight: | 290.83 g./mol | Molecular Formula: | C₁₇H₂₃ClN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD34563811 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, light-proof |
Product Description:
Used as a precursor in the synthesis of N-heterocyclic carbene (NHC) ligands for transition metal catalysis. These ligands are highly effective in stabilizing catalytic metal centers in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, enabling efficient carbon-carbon bond formation. The bulky mesityl and cyclopentyl groups enhance steric protection and electronic tuning of the carbene, improving catalyst longevity and selectivity. Also employed in organocatalysis and the development of novel catalysts for olefin metathesis and CO2 fixation processes. Its stability and solubility profile make it suitable for use in both homogeneous and supported catalytic systems.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿4,580.00 |
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| 0.250 G | 10-20 days | ฿6,200.00 |
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| 1.000 G | 10-20 days | ฿20,020.00 |
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1-Cyclopentyl-3-mesityl-1H-imidazol-3-ium chloride
Used as a precursor in the synthesis of N-heterocyclic carbene (NHC) ligands for transition metal catalysis. These ligands are highly effective in stabilizing catalytic metal centers in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, enabling efficient carbon-carbon bond formation. The bulky mesityl and cyclopentyl groups enhance steric protection and electronic tuning of the carbene, improving catalyst longevity and selectivity. Also employed in organocatalysis and the development of novel catalysts for olefin metathesis and CO2 fixation processes. Its stability and solubility profile make it suitable for use in both homogeneous and supported catalytic systems.
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