1,3-Bis(2,6-diisopropylphenyl)imidazolium-2-carboxylate
98%
- Product Code: 73213
CAS:
917604-39-8
| Molecular Weight: | 432.61 g./mol | Molecular Formula: | C₂₈H₃₆N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, in an inert gas |
Product Description:
This chemical is primarily utilized as a precursor in the synthesis of N-heterocyclic carbenes (NHCs), which are widely employed as ligands in organometallic chemistry. These ligands are crucial in various catalytic processes, including cross-coupling reactions, olefin metathesis, and hydrogenation reactions. The stability and steric bulk provided by the 2,6-diisopropylphenyl groups make it particularly effective in stabilizing metal centers and enhancing catalytic activity. Additionally, it finds application in the development of ionic liquids and as a catalyst in organic synthesis, where it facilitates the formation of carbon-carbon and carbon-heteroatom bonds. Its role in polymerization reactions, particularly in the production of specialty polymers, is also noteworthy.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿2,740.00 |
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| 1.000 | 10-20 days | ฿9,620.00 |
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1,3-Bis(2,6-diisopropylphenyl)imidazolium-2-carboxylate
This chemical is primarily utilized as a precursor in the synthesis of N-heterocyclic carbenes (NHCs), which are widely employed as ligands in organometallic chemistry. These ligands are crucial in various catalytic processes, including cross-coupling reactions, olefin metathesis, and hydrogenation reactions. The stability and steric bulk provided by the 2,6-diisopropylphenyl groups make it particularly effective in stabilizing metal centers and enhancing catalytic activity. Additionally, it finds application in the development of ionic liquids and as a catalyst in organic synthesis, where it facilitates the formation of carbon-carbon and carbon-heteroatom bonds. Its role in polymerization reactions, particularly in the production of specialty polymers, is also noteworthy.
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