2,3-(4-Formylbenzo)-1,4,7,10,13,16-hexaoxacyclooctadec-2-ene
≥98%(GC)
- Product Code: 86065
CAS:
60835-74-7
| Molecular Weight: | 340.37 g./mol | Molecular Formula: | C₁₇H₂₄O₇ |
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| EC Number: | MDL Number: | MFCD00388882 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, inert gas storage |
Product Description:
This compound is primarily utilized in the field of supramolecular chemistry due to its unique structure, which includes a formyl group and a crown ether moiety. The formyl group allows it to act as a reactive site for further chemical modifications, making it a valuable building block for synthesizing more complex molecules. Its crown ether component is particularly effective in binding alkali metal ions, which makes it useful in the development of ion-selective sensors and membranes. Additionally, it finds applications in the design of molecular machines and switches, where its ability to undergo conformational changes in response to external stimuli is exploited. This chemical is also employed in research focused on host-guest chemistry, where it can encapsulate specific ions or molecules, facilitating studies on molecular recognition and interaction.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿15,651.00 |
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2,3-(4-Formylbenzo)-1,4,7,10,13,16-hexaoxacyclooctadec-2-ene
This compound is primarily utilized in the field of supramolecular chemistry due to its unique structure, which includes a formyl group and a crown ether moiety. The formyl group allows it to act as a reactive site for further chemical modifications, making it a valuable building block for synthesizing more complex molecules. Its crown ether component is particularly effective in binding alkali metal ions, which makes it useful in the development of ion-selective sensors and membranes. Additionally, it finds applications in the design of molecular machines and switches, where its ability to undergo conformational changes in response to external stimuli is exploited. This chemical is also employed in research focused on host-guest chemistry, where it can encapsulate specific ions or molecules, facilitating studies on molecular recognition and interaction.
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