n-Octyl 4,6-Dibromo-3-fluorothieno[3,4-b]thiophene-2-carboxylate

≥94%

Reagent Code: #221602
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CAS Number 1160823-76-6

science Other reagents with same CAS 1160823-76-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 472.23 g/mol
Formula C₁₅H₁₇Br₂FO₂S₂
badge Registry Numbers
MDL Number MFCD19940962
thermostat Physical Properties
Melting Point 53-57°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated thiophene backbone enables efficient cross-coupling reactions, facilitating the construction of conjugated polymer chains with tunable electronic properties. The presence of the ester group aids in solubility and processability during device fabrication. Commonly employed in research settings to optimize charge carrier mobility and light absorption characteristics in thin-film electronic devices.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10mg
10-20 days ฿2,540.00
n-Octyl 4,6-Dibromo-3-fluorothieno[3,4-b]thiophene-2-carboxylate
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Used as an intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated thiophene backbone enables efficient cross-coupling reactions, facilitating the construction of conjugated polymer chains with tunable electronic properties. The presence of the ester group aids in solubility and processability during device fabrication. Commonly employed in research s

Used as an intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated thiophene backbone enables efficient cross-coupling reactions, facilitating the construction of conjugated polymer chains with tunable electronic properties. The presence of the ester group aids in solubility and processability during device fabrication. Commonly employed in research settings to optimize charge carrier mobility and light absorption characteristics in thin-film electronic devices.

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