4-Iodothieno[3,4-c]furan-1,3-dione

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Reagent Code: #200865
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CAS Number 2222337-05-3

science Other reagents with same CAS 2222337-05-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.04 g/mol
Formula C₆HIO₃S
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and functional materials, particularly in the development of conjugated polymers for organic electronics. Its iodine functionality allows for cross-coupling reactions, enabling the construction of complex molecular architectures. Applied in research settings to design electron-accepting units in organic semiconductors and photovoltaic devices. Also explored in the synthesis of bioactive compounds due to the thienofuran core’s presence in some pharmacologically active molecules. Additionally, it serves as a linker or surface modifier in chemical sensors to enhance detection sensitivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,290.00
inventory 250mg
10-20 days ฿13,410.00
inventory 1g
10-20 days ฿41,120.00

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4-Iodothieno[3,4-c]furan-1,3-dione
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Used in organic synthesis as an intermediate for pharmaceuticals and functional materials, particularly in the development of conjugated polymers for organic electronics. Its iodine functionality allows for cross-coupling reactions, enabling the construction of complex molecular architectures. Applied in research settings to design electron-accepting units in organic semiconductors and photovoltaic devices. Also explored in the synthesis of bioactive compounds due to the thienofuran core’s presence in so

Used in organic synthesis as an intermediate for pharmaceuticals and functional materials, particularly in the development of conjugated polymers for organic electronics. Its iodine functionality allows for cross-coupling reactions, enabling the construction of complex molecular architectures. Applied in research settings to design electron-accepting units in organic semiconductors and photovoltaic devices. Also explored in the synthesis of bioactive compounds due to the thienofuran core’s presence in some pharmacologically active molecules. Additionally, it serves as a linker or surface modifier in chemical sensors to enhance detection sensitivity.

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