3,6,9,16,19,22-Hexaoxatricyclo[22.2.2.211,14]triaconta-11,13,24,26,27,29-hexaene-2,10,15,23-tetrone
≥95%
- Product Code: 191935
CAS:
16104-98-6
| Molecular Weight: | 472.4414 g./mol | Molecular Formula: | C₂₄H₂₄O₁₀ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 212-214 °C | Boiling Point: | 803.5±65.0 °C(Predicted) |
| Density: | 1.236±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Used primarily in advanced organic synthesis as a high-strain bridged ether scaffold, this compound serves as a specialized building block in the development of cryptand-like molecular receptors. Its unique polycyclic structure with multiple oxygen bridges enables selective metal ion coordination, making it valuable in designing sensors for alkali and alkaline earth metals. It is also employed in supramolecular chemistry to study host-guest interactions, particularly in non-aqueous environments. Due to its electron-rich framework, it finds use in photoresponsive materials and as a ligand in catalytic systems where steric constraint enhances selectivity. Limited solubility in common solvents restricts broad industrial use, but it remains a niche reagent in academic and pharmaceutical research for constructing complex macrocycles.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | $8,438.24 |
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| 0.250 G | 10-20 days | $16,876.48 |
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3,6,9,16,19,22-Hexaoxatricyclo[22.2.2.211,14]triaconta-11,13,24,26,27,29-hexaene-2,10,15,23-tetrone
Used primarily in advanced organic synthesis as a high-strain bridged ether scaffold, this compound serves as a specialized building block in the development of cryptand-like molecular receptors. Its unique polycyclic structure with multiple oxygen bridges enables selective metal ion coordination, making it valuable in designing sensors for alkali and alkaline earth metals. It is also employed in supramolecular chemistry to study host-guest interactions, particularly in non-aqueous environments. Due to its electron-rich framework, it finds use in photoresponsive materials and as a ligand in catalytic systems where steric constraint enhances selectivity. Limited solubility in common solvents restricts broad industrial use, but it remains a niche reagent in academic and pharmaceutical research for constructing complex macrocycles.
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