2-Bromo-3-hexyl-5-iodothiophene

97%, containing stabilizer copper chips

Reagent Code: #147308
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CAS Number 160096-76-4

science Other reagents with same CAS 160096-76-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.09 g/mol
Formula C₁₀H₁₄BrIS
badge Registry Numbers
MDL Number MFCD15144651
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of conjugated polymers for organic electronics. Its halogen substituents enable cross-coupling reactions such as Suzuki or Stille couplings, making it valuable in constructing complex aromatic systems. Commonly applied in the development of organic semiconductors, field-effect transistors (OFETs), and photovoltaic materials due to its ability to fine-tune electronic properties and enhance charge carrier mobility. The hexyl chain improves solubility in organic solvents, facilitating solution-based processing in thin-film device fabrication.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿533.50
inventory 1g
10-20 days ฿1,479.50

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2-Bromo-3-hexyl-5-iodothiophene
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Used primarily as an intermediate in organic synthesis, especially in the preparation of conjugated polymers for organic electronics. Its halogen substituents enable cross-coupling reactions such as Suzuki or Stille couplings, making it valuable in constructing complex aromatic systems. Commonly applied in the development of organic semiconductors, field-effect transistors (OFETs), and photovoltaic materials due to its ability to fine-tune electronic properties and enhance charge carrier mobility. The he

Used primarily as an intermediate in organic synthesis, especially in the preparation of conjugated polymers for organic electronics. Its halogen substituents enable cross-coupling reactions such as Suzuki or Stille couplings, making it valuable in constructing complex aromatic systems. Commonly applied in the development of organic semiconductors, field-effect transistors (OFETs), and photovoltaic materials due to its ability to fine-tune electronic properties and enhance charge carrier mobility. The hexyl chain improves solubility in organic solvents, facilitating solution-based processing in thin-film device fabrication.

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