1,8:4,5-Naphthalenetetracarboxdiimide

≥95%

Reagent Code: #114164
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CAS Number 5690-24-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.21 g/mol
Formula C₁₄H₆N₂O₄
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MDL Number MFCD00047649
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Storage room temperature

description 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.

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Test Parameter Specification
Appearance Yellow to deep yellow-red crystals or powder
Purity (%) 95%

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days $168.32
inventory 5g
10-20 days $2,142.22
inventory 1g
10-20 days $604.68
inventory 25g
10-20 days $6,331.68
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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