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Specifications of 4-(4-Dibenzofuranyl)benzenamine丨CAS 578027-21-1
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Appearance: |
Light pink to off-white solid |
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Purity (HPLC): |
99.0% min |
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Melting Point: |
118.0℃ to 122.0℃ |
Transport Information of 4-(4-Dibenzofuranyl)benzenamine丨CAS 578027-21-1
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Packing Group |
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H.S. Code |
2932999099304 |
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Stability & Reactivity |
The product is chemically stable under standard ambient conditions (room temperature). |
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Storage |
Tightly closed. Store in a closed, dry, ventilated place |
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Manufacturing Information of 4-(4-Dibenzofuranyl)benzenamine丨CAS 578027-21-1
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Parameter |
Specification |
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Capacity |
Hundreds of kg level |
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Experience |
Production since 2021 |
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Stock |
Applications of 4-(4-Dibenzofuranyl)benzenamine丨CAS 578027-21-1
1. Organic Electronics and Optoelectronic Materials
One of the most important uses of 4-(4-Dibenzofuranyl)benzenamine is as an intermediate or core structure in the development of organic electronic materials, including:
● OLEDs (Organic Light Emitting Diodes):
This compound is widely used in the synthesis of hole-transporting materials (HTMs) and host materials in OLED devices. The presence of both the electron-rich amine group and rigid planar dibenzofuran moiety helps in efficient charge mobility and thermal stability.
● OFETs (Organic Field-Effect Transistors):
Its extended π-conjugation and good film-forming properties make it suitable as a component in organic semiconductors.
● Photovoltaics and Solar Cells:
Used in constructing donor-acceptor architectures to improve light absorption and charge transport in organic photovoltaic (OPV) devices.
2. Advanced Functional Material Synthesis
● Donor–Acceptor Systems:
The amine group functions as an electron donor, while the dibenzofuran core contributes rigidity and planarity-key features for tunable photophysical properties. These systems are useful in fluorescent probes, photodetectors, and chemical sensors.
● High-Performance Polymers:
4-(4-Dibenzofuranyl)benzenamine丨CAS 578027-21-1 serves as a monomer or structural unit for synthesizing aromatic polyimides, polyarylenes, or polybenzofurans with desirable optical or thermal properties.
3. Medicinal Chemistry and Bioorganic Studies (Exploratory)
Although less common than in material science, compounds like 4-(4-Dibenzofuranyl)benzenamine may be evaluated for:
● Drug-like scaffolds: Due to its rigid aromatic system and potential for π–π stacking interactions, it can be explored for enzyme inhibition or receptor binding studies.
● Fluorescent probes and biomarkers: Derivatives with appropriate substitutions could serve in biological imaging applications, thanks to their potential for fluorescence and stability.
4. Synthetic Intermediate
● Building Block in Custom Synthesis:
The compound acts as a versatile intermediate in the synthesis of other N-substituted aromatic amines, dendritic molecules, and heterocyclic structures.
Benefits of 4-(4-Dibenzofuranyl)benzenamine丨CAS 578027-21-1
1. High Thermal and Photostability
● The dibenzofuran structure imparts excellent thermal and oxidative stability, making this molecule highly desirable in high-performance electronic applications.
2. Enhanced Charge Transport
● The para-aniline substitution allows for good hole-transport properties, essential in OLEDs and organic transistors.
3. Strong Fluorescent and Optoelectronic Potential
● It provides strong blue emission, high fluorescence quantum yield, and tunable emission spectra when used in OLED host/dopant systems.
4. Good Processability
● Due to its planar aromatic system and moderate solubility in organic solvents, this compound is suitable for spin coating, vacuum deposition, and other thin-film fabrication techniques.
Conclusion
4-(4-Dibenzofuranyl)benzenamine丨CAS 578027-21-1 is a specialty chemical widely employed in the organic electronics industry, particularly in the design and manufacture of OLEDs, photovoltaic devices, and high-performance polymers. Its combination of structural rigidity, electronic donor properties, and thermal stability makes it a valuable component in advanced materials research. With continued growth in organic semiconductors and flexible electronics, this compound will likely remain essential in developing next-generation optoelectronic devices.

