2-((2-Butyloctyl)thio)thiophene

98%

Reagent Code: #153085
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CAS Number 2093197-82-9

science Other reagents with same CAS 2093197-82-9

blur_circular Chemical Specifications

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Weight 284.52 g/mol
Formula C₁₆H₂₈S₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily as a key intermediate in the synthesis of conjugated polymers for organic electronics. It plays an important role in the development of organic semiconductors, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The molecule’s thiophene ring and alkyl side chains enhance solubility and promote π-π stacking, improving charge carrier mobility in thin-film devices. Its thioether linkage contributes to stability and electronic tuning of the resulting polymer. Commonly employed in research settings for designing high-performance, solution-processable electronic materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,400.00
inventory 1g
10-20 days ฿6,220.00
inventory 5g
10-20 days ฿25,400.00

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2-((2-Butyloctyl)thio)thiophene
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Used primarily as a key intermediate in the synthesis of conjugated polymers for organic electronics. It plays an important role in the development of organic semiconductors, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The molecule’s thiophene ring and alkyl side chains enhance solubility and promote π-π stacking, improving charge carrier mobility in thin-film devices. Its thioether linkage contributes to stability and electronic tuning of the resulting poly

Used primarily as a key intermediate in the synthesis of conjugated polymers for organic electronics. It plays an important role in the development of organic semiconductors, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The molecule’s thiophene ring and alkyl side chains enhance solubility and promote π-π stacking, improving charge carrier mobility in thin-film devices. Its thioether linkage contributes to stability and electronic tuning of the resulting polymer. Commonly employed in research settings for designing high-performance, solution-processable electronic materials.

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