15,16-Diethynyl-2,3,5,6,8,9,11,12-octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecine

98%

Reagent Code: #167390
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CAS Number 680573-26-6

science Other reagents with same CAS 680573-26-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.35 g/mol
Formula C₁₈H₂₀O₅
thermostat Physical Properties
Boiling Point 464.8±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.18±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of macrocyclic compounds for advanced materials and supramolecular chemistry. Its rigid ethynyl-functionalized crown ether-like structure enables selective binding of metal ions, making it valuable in sensor design and catalysis. The alkyne groups allow further functionalization via click chemistry, useful in constructing molecular frameworks for organic electronics and coordination networks. Also explored in pharmaceutical research for targeted drug delivery systems due to its ability to form host-guest complexes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿15,610.00
inventory 100mg
10-20 days ฿26,530.00
inventory 250mg
10-20 days ฿45,100.00

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15,16-Diethynyl-2,3,5,6,8,9,11,12-octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecine
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Used as a key intermediate in the synthesis of macrocyclic compounds for advanced materials and supramolecular chemistry. Its rigid ethynyl-functionalized crown ether-like structure enables selective binding of metal ions, making it valuable in sensor design and catalysis. The alkyne groups allow further functionalization via click chemistry, useful in constructing molecular frameworks for organic electronics and coordination networks. Also explored in pharmaceutical research for targeted drug delivery s

Used as a key intermediate in the synthesis of macrocyclic compounds for advanced materials and supramolecular chemistry. Its rigid ethynyl-functionalized crown ether-like structure enables selective binding of metal ions, making it valuable in sensor design and catalysis. The alkyne groups allow further functionalization via click chemistry, useful in constructing molecular frameworks for organic electronics and coordination networks. Also explored in pharmaceutical research for targeted drug delivery systems due to its ability to form host-guest complexes.

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