5,5′-Bis(tributylstannyl)-2,2′-bithiophene

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Reagent Code: #47973
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CAS Number 171290-94-1

science Other reagents with same CAS 171290-94-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 744.35 g/mol
Formula C₃₂H₅₈S₂Sn₂
badge Registry Numbers
MDL Number MFCD01319063
thermostat Physical Properties
Boiling Point 632.7±65.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.217 g/mL at 25℃
Storage 2-8℃

description Product Description

This chemical is primarily used in the field of organic electronics, particularly in the synthesis of conjugated polymers and small molecules for optoelectronic devices. It serves as a key monomer in the preparation of polythiophenes, which are widely employed in organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The tributylstannyl groups facilitate efficient cross-coupling reactions, such as Stille coupling, enabling the construction of well-defined, high-performance semiconducting materials. Its application is crucial for developing materials with tailored electronic properties, improving device efficiency and stability in advanced electronic applications.

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inventory 1g
10-20 days ฿9,351.00

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5,5′-Bis(tributylstannyl)-2,2′-bithiophene
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This chemical is primarily used in the field of organic electronics, particularly in the synthesis of conjugated polymers and small molecules for optoelectronic devices. It serves as a key monomer in the preparation of polythiophenes, which are widely employed in organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The tributylstannyl groups facilitate efficient cross-coupling reactions, such as Stille coupling, enabling the construction of we

This chemical is primarily used in the field of organic electronics, particularly in the synthesis of conjugated polymers and small molecules for optoelectronic devices. It serves as a key monomer in the preparation of polythiophenes, which are widely employed in organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The tributylstannyl groups facilitate efficient cross-coupling reactions, such as Stille coupling, enabling the construction of well-defined, high-performance semiconducting materials. Its application is crucial for developing materials with tailored electronic properties, improving device efficiency and stability in advanced electronic applications.

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