[1,10]PHENANTHROLINE-2,9-DICARBALDEHYDE
98%
- Product Code: 38757
CAS:
57709-62-3
| Molecular Weight: | 236.23 g./mol | Molecular Formula: | C₁₄H₈N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 230℃ | Boiling Point: | 503.8±45.0 °C(Predicted) |
| Density: | 1.410±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is widely utilized as a chelating agent in the synthesis of metal complexes, particularly in coordination chemistry, due to its ability to form stable complexes with various metal ions. It serves as a key building block in the development of luminescent materials, where its derivatives are employed in the design of organic light-emitting diodes (OLEDs) and sensors for detecting metal ions. Additionally, it is used in supramolecular chemistry for constructing molecular frameworks and host-guest systems. Its aldehyde groups enable further functionalization, making it valuable in the preparation of Schiff bases and other organic compounds for applications in catalysis and material science.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Yellow solid powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $80.86 |
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| 0.500 | 10-20 days | $279.76 |
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| 1.000 | 10-20 days | $385.74 |
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[1,10]PHENANTHROLINE-2,9-DICARBALDEHYDE
This chemical is widely utilized as a chelating agent in the synthesis of metal complexes, particularly in coordination chemistry, due to its ability to form stable complexes with various metal ions. It serves as a key building block in the development of luminescent materials, where its derivatives are employed in the design of organic light-emitting diodes (OLEDs) and sensors for detecting metal ions. Additionally, it is used in supramolecular chemistry for constructing molecular frameworks and host-guest systems. Its aldehyde groups enable further functionalization, making it valuable in the preparation of Schiff bases and other organic compounds for applications in catalysis and material science.
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