3-(Pent-4-en-1-yl)thiophene

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Reagent Code: #227557
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CAS Number 235088-75-2

science Other reagents with same CAS 235088-75-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.26 g/mol
Formula C₉H₁₂S
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as a key intermediate in organic synthesis, particularly in the production of conjugated polymers for organic electronics such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its vinyl-terminated side chain enables further functionalization via cross-coupling reactions or polymerization, making it valuable in constructing pi-conjugated systems. Also employed in the development of specialty monomers for copolymerization processes aimed at tuning the electronic and optical properties of materials. Its thiophene core contributes to electron-rich character, enhancing charge transport in semiconductor materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,060.00
inventory 250mg
10-20 days ฿6,070.00
inventory 1g
10-20 days ฿19,600.00

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3-(Pent-4-en-1-yl)thiophene
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Used as a key intermediate in organic synthesis, particularly in the production of conjugated polymers for organic electronics such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its vinyl-terminated side chain enables further functionalization via cross-coupling reactions or polymerization, making it valuable in constructing pi-conjugated systems. Also employed in the development of specialty monomers for copolymerization processes aimed at tuning the electronic and optica

Used as a key intermediate in organic synthesis, particularly in the production of conjugated polymers for organic electronics such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its vinyl-terminated side chain enables further functionalization via cross-coupling reactions or polymerization, making it valuable in constructing pi-conjugated systems. Also employed in the development of specialty monomers for copolymerization processes aimed at tuning the electronic and optical properties of materials. Its thiophene core contributes to electron-rich character, enhancing charge transport in semiconductor materials.

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