1,2-Diethynylbenzene

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Reagent Code: #178498
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CAS Number 21792-52-9

science Other reagents with same CAS 21792-52-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 126.15 g/mol
Formula C₁₀H₆
inventory_2 Storage & Handling
Storage -20°C, dry

description Product Description

Used as a building block in organic synthesis, particularly in the preparation of conjugated polymers and molecular wires due to its rigid aromatic backbone and reactive ethynyl groups. It plays a key role in cross-coupling reactions, such as Sonogashira coupling, enabling the construction of extended π-systems for optoelectronic materials. Also employed in the development of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs), where its linear geometry and reactivity help form porous, stable networks. Additionally, it serves as a precursor in synthesizing carbon-rich compounds and nanostructures, including graphene-like materials and carbon nanotubes, through controlled cyclization and polymerization processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,880.00
inventory 250mg
10-20 days ฿6,200.00
inventory 1g
10-20 days ฿16,040.00
inventory 5g
10-20 days ฿58,740.00

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1,2-Diethynylbenzene
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Used as a building block in organic synthesis, particularly in the preparation of conjugated polymers and molecular wires due to its rigid aromatic backbone and reactive ethynyl groups. It plays a key role in cross-coupling reactions, such as Sonogashira coupling, enabling the construction of extended π-systems for optoelectronic materials. Also employed in the development of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs), where its linear geometry and reactivity help form porous,

Used as a building block in organic synthesis, particularly in the preparation of conjugated polymers and molecular wires due to its rigid aromatic backbone and reactive ethynyl groups. It plays a key role in cross-coupling reactions, such as Sonogashira coupling, enabling the construction of extended π-systems for optoelectronic materials. Also employed in the development of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs), where its linear geometry and reactivity help form porous, stable networks. Additionally, it serves as a precursor in synthesizing carbon-rich compounds and nanostructures, including graphene-like materials and carbon nanotubes, through controlled cyclization and polymerization processes.

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