Tributyl(3-(2-butyloctyl)thiophen-2-yl)stannane

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Reagent Code: #242942
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CAS Number 1640126-30-2

science Other reagents with same CAS 1640126-30-2

blur_circular Chemical Specifications

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Weight 541.50 g/mol
Formula C₂₈H₅₄SSn
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used primarily as a reagent in organic synthesis, especially in Stille coupling reactions, enabling the formation of carbon-carbon bonds in the production of conjugated organic materials. It is particularly valuable in the synthesis of organic semiconductors and advanced polymers used in electronic devices such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The compound facilitates the introduction of thiophene-based moieties into larger aromatic systems, enhancing electronic properties and material stability. Its application supports the development of flexible electronics and printed circuit technologies due to improved solubility and processability of resulting materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,370.00
inventory 250mg
10-20 days ฿5,580.00
inventory 1g
10-20 days ฿18,000.00

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Tributyl(3-(2-butyloctyl)thiophen-2-yl)stannane
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Used primarily as a reagent in organic synthesis, especially in Stille coupling reactions, enabling the formation of carbon-carbon bonds in the production of conjugated organic materials. It is particularly valuable in the synthesis of organic semiconductors and advanced polymers used in electronic devices such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The compound facilitates the introduction of thiophene-based moieties into larger aromatic systems, enhancing electron

Used primarily as a reagent in organic synthesis, especially in Stille coupling reactions, enabling the formation of carbon-carbon bonds in the production of conjugated organic materials. It is particularly valuable in the synthesis of organic semiconductors and advanced polymers used in electronic devices such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The compound facilitates the introduction of thiophene-based moieties into larger aromatic systems, enhancing electronic properties and material stability. Its application supports the development of flexible electronics and printed circuit technologies due to improved solubility and processability of resulting materials.

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