3,3',5,5'-Tetrabromo-2,2'-bithiophene

98%

Reagent Code: #240763
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CAS Number 125143-53-5

science Other reagents with same CAS 125143-53-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 481.85 g/mol
Formula C₈H₂Br₄S₂
badge Registry Numbers
MDL Number MFCD00114807
thermostat Physical Properties
Melting Point 138-143°C
Boiling Point 371°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic semiconductor synthesis, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated structure allows for efficient cross-coupling reactions, enabling precise molecular engineering of π-conjugated systems. The compound contributes to enhancing charge carrier mobility and thermal stability in thin-film electronic devices. Also explored in the synthesis of specialty dyes and fluorescent probes due to its rigid bithiophene backbone and halogenation pattern.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿148.50
inventory 5g
10-20 days ฿500.00
inventory 100g
10-20 days ฿8,560.00
inventory 500g
10-20 days ฿42,000.00
inventory 1g
10-20 days ฿165.00
inventory 25g
10-20 days ฿2,200.00
3,3',5,5'-Tetrabromo-2,2'-bithiophene
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Used as an intermediate in organic semiconductor synthesis, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated structure allows for efficient cross-coupling reactions, enabling precise molecular engineering of π-conjugated systems. The compound contributes to enhancing charge carrier mobility and thermal stability in thin-film electronic devices. Also explored in the synthesis of specialty dyes and fluorescent
Used as an intermediate in organic semiconductor synthesis, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated structure allows for efficient cross-coupling reactions, enabling precise molecular engineering of π-conjugated systems. The compound contributes to enhancing charge carrier mobility and thermal stability in thin-film electronic devices. Also explored in the synthesis of specialty dyes and fluorescent probes due to its rigid bithiophene backbone and halogenation pattern.
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