(1-Ethynylanthracene-9,10-diyl)bis(trimethylsilane)

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Reagent Code: #180758
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CAS Number 2807490-29-3

science Other reagents with same CAS 2807490-29-3

blur_circular Chemical Specifications

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Weight 346.61 g/mol
Formula C₂₂H₂₆Si₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of conjugated organic semiconductors and optoelectronic materials. Its rigid anthracene backbone and ethynyl functionality enable efficient π-conjugation, making it valuable in the development of organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs). The trimethylsilyl groups enhance solubility and stability during synthetic processing, allowing for easier purification and handling in air-sensitive reactions. It is also employed in Sonogashira coupling reactions to build extended aromatic systems for photovoltaic applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,950.00
inventory 1g
10-20 days ฿5,240.00
inventory 5g
10-20 days ฿18,320.00

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(1-Ethynylanthracene-9,10-diyl)bis(trimethylsilane)
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Used as a key intermediate in the synthesis of conjugated organic semiconductors and optoelectronic materials. Its rigid anthracene backbone and ethynyl functionality enable efficient π-conjugation, making it valuable in the development of organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs). The trimethylsilyl groups enhance solubility and stability during synthetic processing, allowing for easier purification and handling in air-sensitive reactions. It is also employed in Sonogash

Used as a key intermediate in the synthesis of conjugated organic semiconductors and optoelectronic materials. Its rigid anthracene backbone and ethynyl functionality enable efficient π-conjugation, making it valuable in the development of organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs). The trimethylsilyl groups enhance solubility and stability during synthetic processing, allowing for easier purification and handling in air-sensitive reactions. It is also employed in Sonogashira coupling reactions to build extended aromatic systems for photovoltaic applications.

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