Tributyl(4-(2-ethylhexyl)thiophen-2-yl)stannane

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Reagent Code: #128577
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CAS Number 886746-54-9

science Other reagents with same CAS 886746-54-9

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Weight 485.4 g/mol
Formula C₂₄H₄₆SSn
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Storage Room temperature

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Used primarily as a precursor in organic synthesis, especially in the preparation of conjugated polymers and small molecule semiconductors for organic electronics. Its stannane functionality enables efficient Stille coupling reactions, allowing for the formation of carbon–carbon bonds in the synthesis of complex π-conjugated systems. Commonly applied in the development of organic photovoltaics (OPVs), organic light-emitting diodes (OLEDs), and organic field-effect transistors (OFETs). The presence of the thiophene ring enhances electronic properties, promoting charge transport in thin-film devices. Its solubility in common organic solvents facilitates solution-processing techniques, making it suitable for large-area and flexible electronic applications.

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inventory 5g
10-20 days ฿29,000.00

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Tributyl(4-(2-ethylhexyl)thiophen-2-yl)stannane
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Used primarily as a precursor in organic synthesis, especially in the preparation of conjugated polymers and small molecule semiconductors for organic electronics. Its stannane functionality enables efficient Stille coupling reactions, allowing for the formation of carbon–carbon bonds in the synthesis of complex π-conjugated systems. Commonly applied in the development of organic photovoltaics (OPVs), organic light-emitting diodes (OLEDs), and organic field-effect transistors (OFETs). The presence of the

Used primarily as a precursor in organic synthesis, especially in the preparation of conjugated polymers and small molecule semiconductors for organic electronics. Its stannane functionality enables efficient Stille coupling reactions, allowing for the formation of carbon–carbon bonds in the synthesis of complex π-conjugated systems. Commonly applied in the development of organic photovoltaics (OPVs), organic light-emitting diodes (OLEDs), and organic field-effect transistors (OFETs). The presence of the thiophene ring enhances electronic properties, promoting charge transport in thin-film devices. Its solubility in common organic solvents facilitates solution-processing techniques, making it suitable for large-area and flexible electronic applications.

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