1-(2,4,6-Trimethylphenyl)-3-(adamantyl)imidazolium chloride
98%
- Product Code: 69018
CAS:
1583244-07-8
Molecular Weight: | 356.93 g./mol | Molecular Formula: | C₂₂H₂₉ClN₂ |
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EC Number: | MDL Number: | MFCD28139678 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a catalyst, particularly in reactions involving the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure, combining an imidazolium core with adamantyl and trimethylphenyl groups, enhances its stability and reactivity under various conditions. It is often employed in ionic liquid applications, where it serves as a solvent or co-solvent in catalytic processes, improving reaction efficiency and selectivity. Additionally, it finds use in the development of advanced materials, such as polymers and coatings, where its ionic properties contribute to improved performance and durability. In medicinal chemistry, it is explored for its potential as a precursor in the synthesis of biologically active molecules, leveraging its structural complexity to target specific interactions.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿4,122.00 |
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0.250 | 10-20 days | ฿6,993.00 |
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1.000 | 10-20 days | ฿18,162.00 |
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1-(2,4,6-Trimethylphenyl)-3-(adamantyl)imidazolium chloride
This compound is primarily utilized in the field of organic synthesis as a catalyst, particularly in reactions involving the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure, combining an imidazolium core with adamantyl and trimethylphenyl groups, enhances its stability and reactivity under various conditions. It is often employed in ionic liquid applications, where it serves as a solvent or co-solvent in catalytic processes, improving reaction efficiency and selectivity. Additionally, it finds use in the development of advanced materials, such as polymers and coatings, where its ionic properties contribute to improved performance and durability. In medicinal chemistry, it is explored for its potential as a precursor in the synthesis of biologically active molecules, leveraging its structural complexity to target specific interactions.
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