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%

Reagent Code: #191935
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CAS Number 16104-98-6

science Other reagents with same CAS 16104-98-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 472.4414 g/mol
Formula C₂₄H₂₄O₁₀
thermostat Physical Properties
Melting Point 212-214 °C
Boiling Point 803.5±65.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.236±0.06 g/cm3(Predicted)
Storage 2-8°C

description 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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿160,000.00
250mg
10-20 days ฿320,000.00
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
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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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