2,5-Dibromo-3,4-thiophenedicarboxylic Anhydride

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Reagent Code: #174800
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CAS Number 1015423-45-6

science Other reagents with same CAS 1015423-45-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.93 g/mol
Formula C₆Br₂O₃S
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of conjugated organic semiconductors, particularly in the development of high-performance organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid aromatic structure and strong electron-withdrawing nature enhance charge carrier mobility and stability in thin-film devices. Also employed in the preparation of functional dyes and fluorescent probes due to its ability to participate in π-conjugated systems with tunable optical properties. Commonly utilized in cross-coupling reactions to build complex heterocyclic frameworks for optoelectronic materials.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,750.00
inventory 250mg
10-20 days ฿5,600.00
inventory 1g
10-20 days ฿8,430.00

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2,5-Dibromo-3,4-thiophenedicarboxylic Anhydride
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Used as a key intermediate in the synthesis of conjugated organic semiconductors, particularly in the development of high-performance organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid aromatic structure and strong electron-withdrawing nature enhance charge carrier mobility and stability in thin-film devices. Also employed in the preparation of functional dyes and fluorescent probes due to its ability to participate in π-conjugated systems with tunable optical properties

Used as a key intermediate in the synthesis of conjugated organic semiconductors, particularly in the development of high-performance organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid aromatic structure and strong electron-withdrawing nature enhance charge carrier mobility and stability in thin-film devices. Also employed in the preparation of functional dyes and fluorescent probes due to its ability to participate in π-conjugated systems with tunable optical properties. Commonly utilized in cross-coupling reactions to build complex heterocyclic frameworks for optoelectronic materials.

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