1-(2,4,6-Trimethylphenyl)-3-[(1R,2R,3R,5S)-(-)-isopinocampheyl]imidazolium chloride
≥95%
- Product Code: 70574
CAS:
1583244-12-5
| Molecular Weight: | 358.95 g./mol | Molecular Formula: | C₂₂H₃₁ClN₂ |
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| EC Number: | MDL Number: | MFCD28144534 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This compound is primarily utilized as a chiral ionic liquid or catalyst in asymmetric synthesis, particularly in organic transformations where enantioselectivity is crucial. Its unique structure, combining an imidazolium core with a chiral isopinocampheyl group, makes it effective in facilitating stereocontrolled reactions such as hydrogenation, cyclopropanation, and Diels-Alder reactions. It is also employed in the development of chiral materials and as a phase-transfer catalyst in biphasic systems, enhancing reaction efficiency and selectivity. Additionally, its application extends to the field of green chemistry, where it serves as a reusable and environmentally friendly alternative to traditional catalysts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,829.00 |
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1-(2,4,6-Trimethylphenyl)-3-[(1R,2R,3R,5S)-(-)-isopinocampheyl]imidazolium chloride
This compound is primarily utilized as a chiral ionic liquid or catalyst in asymmetric synthesis, particularly in organic transformations where enantioselectivity is crucial. Its unique structure, combining an imidazolium core with a chiral isopinocampheyl group, makes it effective in facilitating stereocontrolled reactions such as hydrogenation, cyclopropanation, and Diels-Alder reactions. It is also employed in the development of chiral materials and as a phase-transfer catalyst in biphasic systems, enhancing reaction efficiency and selectivity. Additionally, its application extends to the field of green chemistry, where it serves as a reusable and environmentally friendly alternative to traditional catalysts.
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