(5-(2-Ethylhexyl)thiophen-2-yl)trimethylstannane

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Reagent Code: #184663
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CAS Number 1429306-71-7

science Other reagents with same CAS 1429306-71-7

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Weight 359.16 g/mol
Formula C₁₅H₂₈SSn
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MDL Number MFCD30541541
inventory_2 Storage & Handling
Storage 2-8°C, away from light, dry

description Product Description

Used primarily as a reagent in organic synthesis, especially in Stille coupling reactions, where it serves to introduce conjugated thiophene units into larger aromatic or conjugated systems. This application is particularly valuable in the development of organic semiconductors, including materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The presence of the 2-ethylhexyl group enhances solubility in organic solvents, which improves processability and film formation in electronic devices. Its tin moiety enables efficient cross-coupling under palladium catalysis, making it a useful building block for constructing complex π-conjugated structures with tailored electronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,500.00

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(5-(2-Ethylhexyl)thiophen-2-yl)trimethylstannane
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Used primarily as a reagent in organic synthesis, especially in Stille coupling reactions, where it serves to introduce conjugated thiophene units into larger aromatic or conjugated systems. This application is particularly valuable in the development of organic semiconductors, including materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The presence of the 2-ethylhexyl group enhances solubility in organic solvents, which improves processability and film formation in el
Used primarily as a reagent in organic synthesis, especially in Stille coupling reactions, where it serves to introduce conjugated thiophene units into larger aromatic or conjugated systems. This application is particularly valuable in the development of organic semiconductors, including materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The presence of the 2-ethylhexyl group enhances solubility in organic solvents, which improves processability and film formation in electronic devices. Its tin moiety enables efficient cross-coupling under palladium catalysis, making it a useful building block for constructing complex π-conjugated structures with tailored electronic properties.
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