2,5-DIbromo-3,4-dimethyl-thiophene

95%

Reagent Code: #177412
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CAS Number 74707-05-4

science Other reagents with same CAS 74707-05-4

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Weight 269.98 g/mol
Formula C₆H₆Br₂S
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MDL Number MFCD13193229
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the production of conjugated polymers for organic electronics such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated structure allows for palladium-catalyzed cross-coupling reactions, enabling the construction of complex conjugated systems. The presence of methyl groups enhances solubility and influences molecular packing, which can improve charge carrier mobility in semiconductor materials. It is also employed in the synthesis of functionalized thiophene-based small molecules for optoelectronic applications and sensor development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,560.00
inventory 250mg
10-20 days ฿17,100.00
inventory 1g
10-20 days ฿34,200.00

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2,5-DIbromo-3,4-dimethyl-thiophene
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Used primarily as an intermediate in organic synthesis, especially in the production of conjugated polymers for organic electronics such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated structure allows for palladium-catalyzed cross-coupling reactions, enabling the construction of complex conjugated systems. The presence of methyl groups enhances solubility and influences molecular packing, which can improve charge carrier mobility in semiconductor materials. I

Used primarily as an intermediate in organic synthesis, especially in the production of conjugated polymers for organic electronics such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated structure allows for palladium-catalyzed cross-coupling reactions, enabling the construction of complex conjugated systems. The presence of methyl groups enhances solubility and influences molecular packing, which can improve charge carrier mobility in semiconductor materials. It is also employed in the synthesis of functionalized thiophene-based small molecules for optoelectronic applications and sensor development.

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