2-Bromo-3-(2-ethylhexyl)-5-iodothiophene

≥97%, containing stabilizer copper chips

Reagent Code: #147295
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CAS Number 1034352-30-1

science Other reagents with same CAS 1034352-30-1

blur_circular Chemical Specifications

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Weight 401.14 g/mol
Formula C₁₂H₁₈BrIS
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 and small molecule semiconductors for organic electronics. Its halogen substituents enable cross-coupling reactions such as Suzuki or Stille couplings, allowing for the construction of complex π-conjugated systems. Commonly employed in the development of organic photovoltaics (OPVs) and organic field-effect transistors (OFETs) due to its ability to fine-tune electronic properties and enhance charge carrier mobility when incorporated into donor-acceptor materials. The presence of both bromine and iodine offers selective reactivity, facilitating stepwise functionalization in multi-step syntheses. The 2-ethylhexyl substituent enhances solubility in organic solvents, making it suitable for thin-film processing in device fabrication.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,000.00
inventory 1g
10-20 days ฿3,000.00

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2-Bromo-3-(2-ethylhexyl)-5-iodothiophene
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Used primarily as an intermediate in organic synthesis, especially in the preparation of conjugated polymers and small molecule semiconductors for organic electronics. Its halogen substituents enable cross-coupling reactions such as Suzuki or Stille couplings, allowing for the construction of complex π-conjugated systems. Commonly employed in the development of organic photovoltaics (OPVs) and organic field-effect transistors (OFETs) due to its ability to fine-tune electronic properties and enhance charg

Used primarily as an intermediate in organic synthesis, especially in the preparation of conjugated polymers and small molecule semiconductors for organic electronics. Its halogen substituents enable cross-coupling reactions such as Suzuki or Stille couplings, allowing for the construction of complex π-conjugated systems. Commonly employed in the development of organic photovoltaics (OPVs) and organic field-effect transistors (OFETs) due to its ability to fine-tune electronic properties and enhance charge carrier mobility when incorporated into donor-acceptor materials. The presence of both bromine and iodine offers selective reactivity, facilitating stepwise functionalization in multi-step syntheses. The 2-ethylhexyl substituent enhances solubility in organic solvents, making it suitable for thin-film processing in device fabrication.

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