1,8:4,5-Naphthalenetetracarboxdiimide
≥95%
- Product Code: 114164
CAS:
5690-24-4
Molecular Weight: | 266.21 g./mol | Molecular Formula: | C₁₄H₆N₂O₄ |
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EC Number: | MDL Number: | MFCD00047649 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
Widely used in organic electronics due to its electron-accepting properties, this compound is essential in the development of n-type semiconductors for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ability to stabilize negative charges makes it a key component in the design of high-performance electronic devices. Additionally, it is employed in the synthesis of dyes and pigments, offering strong colorfastness and stability. In material science, it serves as a building block for supramolecular assemblies and coordination polymers, leveraging its planar structure and intermolecular interactions. Its applications also extend to molecular sensors, where it is used to detect anions and neutral molecules through selective binding.
Product Specification:
Test | Specification |
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Appearance | Yellow To Deep Yellow Red Crystal Or Powder |
Purity (%) | 95 |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | ฿3,190.00 |
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1.000 | 10-20 days | ฿11,460.00 |
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5.000 | 10-20 days | ฿40,600.00 |
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25.000 | 10-20 days | ฿120,000.00 |
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1,8:4,5-Naphthalenetetracarboxdiimide
Widely used in organic electronics due to its electron-accepting properties, this compound is essential in the development of n-type semiconductors for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ability to stabilize negative charges makes it a key component in the design of high-performance electronic devices. Additionally, it is employed in the synthesis of dyes and pigments, offering strong colorfastness and stability. In material science, it serves as a building block for supramolecular assemblies and coordination polymers, leveraging its planar structure and intermolecular interactions. Its applications also extend to molecular sensors, where it is used to detect anions and neutral molecules through selective binding.
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