2,5-di(1H-imidazol-1-yl)terephthalic acid
98%
- Product Code: 40867
CAS:
1942879-46-0
| Molecular Weight: | 298.2536 g./mol | Molecular Formula: | C₁₄H₁₀N₄O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 632.1±55.0℃(Predicted) | |
| Density: | 1.54±0.1g/ml(Predicted) | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in the development of advanced materials, particularly in the synthesis of metal-organic frameworks (MOFs). Its structure allows it to act as a versatile ligand, forming stable coordination polymers with various metal ions. These MOFs are employed in gas storage and separation processes, such as capturing carbon dioxide or storing hydrogen, due to their high porosity and surface area. Additionally, it finds applications in catalysis, where it serves as a scaffold for designing efficient catalytic systems for organic transformations. Its imidazole groups also make it suitable for use in proton-conducting materials, which are essential in fuel cell technologies. Furthermore, it is explored in the field of sensing, where its ability to interact with specific analytes enables the detection of gases or small molecules.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,690.00 |
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| 1.000 | 10-20 days | ฿12,360.00 |
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2,5-di(1H-imidazol-1-yl)terephthalic acid
This chemical is primarily utilized in the development of advanced materials, particularly in the synthesis of metal-organic frameworks (MOFs). Its structure allows it to act as a versatile ligand, forming stable coordination polymers with various metal ions. These MOFs are employed in gas storage and separation processes, such as capturing carbon dioxide or storing hydrogen, due to their high porosity and surface area. Additionally, it finds applications in catalysis, where it serves as a scaffold for designing efficient catalytic systems for organic transformations. Its imidazole groups also make it suitable for use in proton-conducting materials, which are essential in fuel cell technologies. Furthermore, it is explored in the field of sensing, where its ability to interact with specific analytes enables the detection of gases or small molecules.
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