Diethyl 4,4'-(ethyne-1,2-diyl)dibenzoate

98%

Reagent Code: #178766
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CAS Number 83536-13-4

science Other reagents with same CAS 83536-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.36 g/mol
Formula C₂₀H₁₈O₄
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key monomer in organic synthesis, particularly in the preparation of conjugated polymers for optoelectronic devices. Its rigid ethynylene backbone and ester functional groups enable efficient π-conjugation, making it valuable in the development of organic semiconductors, light-emitting diodes (OLEDs), and photovoltaic materials. The compound participates in palladium-catalyzed coupling reactions to build extended aromatic systems. It is also employed in the synthesis of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) due to its ability to form stable, porous structures with defined geometry. Its linear, symmetrical structure supports the design of materials with high thermal stability and tunable electronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿980.00
inventory 1g
10-20 days ฿2,720.00
inventory 5g
10-20 days ฿11,660.00
inventory 250mg
10-20 days ฿1,100.00
inventory 10g
10-20 days ฿23,300.00

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Diethyl 4,4'-(ethyne-1,2-diyl)dibenzoate
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Used as a key monomer in organic synthesis, particularly in the preparation of conjugated polymers for optoelectronic devices. Its rigid ethynylene backbone and ester functional groups enable efficient π-conjugation, making it valuable in the development of organic semiconductors, light-emitting diodes (OLEDs), and photovoltaic materials. The compound participates in palladium-catalyzed coupling reactions to build extended aromatic systems. It is also employed in the synthesis of metal-organic frameworks

Used as a key monomer in organic synthesis, particularly in the preparation of conjugated polymers for optoelectronic devices. Its rigid ethynylene backbone and ester functional groups enable efficient π-conjugation, making it valuable in the development of organic semiconductors, light-emitting diodes (OLEDs), and photovoltaic materials. The compound participates in palladium-catalyzed coupling reactions to build extended aromatic systems. It is also employed in the synthesis of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) due to its ability to form stable, porous structures with defined geometry. Its linear, symmetrical structure supports the design of materials with high thermal stability and tunable electronic properties.

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