2,3,6,7-tetra-(2-ethoxycarbonylbenzene)tetrathiafulvalene

95%

Reagent Code: #239083
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CAS Number 1356336-61-2

science Other reagents with same CAS 1356336-61-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 797.01 g/mol
Formula C₄₂H₃₆O₈S₄
badge Registry Numbers
MDL Number MFCD31630426
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily in organic electronics, this compound serves as a key building block in the development of organic semiconductors and conductive materials. Its extended π-conjugated system, combined with electron-rich tetrathiafulvalene core and ester-functionalized aryl groups, enables efficient charge transport and tunable redox properties. It is employed in the fabrication of organic field-effect transistors (OFETs) and molecular-scale electronic devices where stable and reversible oxidation behavior is required. Additionally, it finds use in supramolecular chemistry for constructing charge-transfer complexes and in studies related to molecular recognition and self-assembly due to its ability to form donor-acceptor systems. The ester functionalities allow further chemical modification or anchoring to surfaces, making it suitable for use in molecular electronics and sensor platforms.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,800.00
inventory 250mg
10-20 days ฿19,440.00
inventory 1g
10-20 days ฿58,320.00
2,3,6,7-tetra-(2-ethoxycarbonylbenzene)tetrathiafulvalene
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Used primarily in organic electronics, this compound serves as a key building block in the development of organic semiconductors and conductive materials. Its extended π-conjugated system, combined with electron-rich tetrathiafulvalene core and ester-functionalized aryl groups, enables efficient charge transport and tunable redox properties. It is employed in the fabrication of organic field-effect transistors (OFETs) and molecular-scale electronic devices where stable and reversible oxidation behavior i

Used primarily in organic electronics, this compound serves as a key building block in the development of organic semiconductors and conductive materials. Its extended π-conjugated system, combined with electron-rich tetrathiafulvalene core and ester-functionalized aryl groups, enables efficient charge transport and tunable redox properties. It is employed in the fabrication of organic field-effect transistors (OFETs) and molecular-scale electronic devices where stable and reversible oxidation behavior is required. Additionally, it finds use in supramolecular chemistry for constructing charge-transfer complexes and in studies related to molecular recognition and self-assembly due to its ability to form donor-acceptor systems. The ester functionalities allow further chemical modification or anchoring to surfaces, making it suitable for use in molecular electronics and sensor platforms.

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