3-Bromo-6-Iodothieno[3,2-B]Thiophene

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Reagent Code: #154102
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CAS Number 1394840-27-7

science Other reagents with same CAS 1394840-27-7

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Weight 345.02 g/mol
Formula C₆H₂BrIS₂
inventory_2 Storage & Handling
Storage Room temperature

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Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its halogenated structure allows for selective cross-coupling reactions, enabling precise molecular engineering of π-conjugated systems. Commonly employed in Suzuki and Stille coupling reactions to build complex thiophene-based frameworks with enhanced charge transport properties. Also explored in the fabrication of high-performance thin-film transistors and flexible electronic devices due to its strong intermolecular interactions and planar molecular geometry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿850.00
inventory 250mg
10-20 days ฿1,430.00
inventory 1g
10-20 days ฿2,630.00
inventory 5g
10-20 days ฿9,540.00
inventory 10g
10-20 days ฿17,410.00

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3-Bromo-6-Iodothieno[3,2-B]Thiophene
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Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its halogenated structure allows for selective cross-coupling reactions, enabling precise molecular engineering of π-conjugated systems. Commonly employed in Suzuki and Stille coupling reactions to build complex thiophene-based frameworks with enhanced charge transport properties. Also explored in the f

Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its halogenated structure allows for selective cross-coupling reactions, enabling precise molecular engineering of π-conjugated systems. Commonly employed in Suzuki and Stille coupling reactions to build complex thiophene-based frameworks with enhanced charge transport properties. Also explored in the fabrication of high-performance thin-film transistors and flexible electronic devices due to its strong intermolecular interactions and planar molecular geometry.

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