4,4',4'',4'''-(6,7,9,10,17,18,20,21-Octahydrodibenzo[b,k][1,4,7,10,13,16]hexaoxacyclooctadecine-2,3,13,14-tetrayl)tetrabenzaldehyde

98% (contains ~10%solvents)

Reagent Code: #220985
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CAS Number 2837061-91-1

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 776.83 g/mol
Formula C₄₈H₄₀O₁₀
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a multifunctional crosslinking agent in advanced polymer synthesis, particularly for covalent organic frameworks (COFs) and porous organic frameworks. Its four aldehyde groups enable robust Schiff base reactions with amine-functionalized building blocks, forming highly ordered, nitrogen-rich network structures with high surface area and tunable pore sizes, applied in gas storage, catalysis, and environmental remediation. The integrated dibenzo-18-crown-6-like ether structure enhances selective binding of metal ions, supporting supramolecular chemistry, chemical sensors, and controlled drug delivery systems. Additionally, the extended aromatic system aids in fluorescence quenching or analyte selectivity for sensing platforms.

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Size Availability Unit Price Quantity
inventory 100 mg
10-20 days ฿7,560.00
inventory 250 mg
10-20 days ฿11,250.00
inventory 1 g
10-20 days ฿28,400.00

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4,4',4'',4'''-(6,7,9,10,17,18,20,21-Octahydrodibenzo[b,k][1,4,7,10,13,16]hexaoxacyclooctadecine-2,3,13,14-tetrayl)tetrabenzaldehyde
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Used as a multifunctional crosslinking agent in advanced polymer synthesis, particularly for covalent organic frameworks (COFs) and porous organic frameworks. Its four aldehyde groups enable robust Schiff base reactions with amine-functionalized building blocks, forming highly ordered, nitrogen-rich network structures with high surface area and tunable pore sizes, applied in gas storage, catalysis, and environmental remediation. The integrated dibenzo-18-crown-6-like ether structure enhances selective bi

Used as a multifunctional crosslinking agent in advanced polymer synthesis, particularly for covalent organic frameworks (COFs) and porous organic frameworks. Its four aldehyde groups enable robust Schiff base reactions with amine-functionalized building blocks, forming highly ordered, nitrogen-rich network structures with high surface area and tunable pore sizes, applied in gas storage, catalysis, and environmental remediation. The integrated dibenzo-18-crown-6-like ether structure enhances selective binding of metal ions, supporting supramolecular chemistry, chemical sensors, and controlled drug delivery systems. Additionally, the extended aromatic system aids in fluorescence quenching or analyte selectivity for sensing platforms.

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