2,3,6,7-tetra-(2-ethoxycarbonylbenzene)tetrathiafulvalene
95%
- Product Code: 239083
CAS:
1356336-61-2
| Molecular Weight: | 797.01 g./mol | Molecular Formula: | C₄₂H₃₆O₈S₄ |
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| EC Number: | MDL Number: | MFCD31630426 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
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.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 100mg | 10-20 days | $332.99 |
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| 250mg | 10-20 days | $599.37 |
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| bulk | 10-20 days | $0.00 |
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| 1g | 10-20 days | $1,798.12 |
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2,3,6,7-tetra-(2-ethoxycarbonylbenzene)tetrathiafulvalene
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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