9,10-Bis(4-formylphenyl)anthracene
CAS Number 324750-99-4
Carbaldehyde Monomers, Chemistry Building Blocks, COF Ligands, Materials, Monomers, Porous Organic Frameworks
Covalent Organic Frameworks (COFs) Anthracene Ligand
A formyl functional ligand linker for COFs in application of nitrofuran and nitroaromatic explosive detection, photo sterilisation and OLEDs
9,10-Bis(4-formylphenyl)anthracene (BFPA), CAS number 324750-99-4, has an anthracene core with two 4-formylphenyl groups at 9,10-positions. Anthracene derivatives are important sources of singlet oxygen (1O2).
Porphyrin–anthracene covalent organic framework, Por-DPA-COF, was constructed by using a porphyrin photosensitizer as the active nodes to provide photothermal and photodynamic activities under irradiation, and 9,10-bis(4-formylphenyl)anthracene as the linkage to capture 1O2 and release it in the dark. Por-DPA-COF exhibited good photothermal conversion performance and efficient 1O2 production capacity thus promoting wound healing without obvious side effects as a novel efficient bactericide.
Luminescent conjugated microporous polymer (AP-CMP), through the polycondensation of 9,10-bis(4-formylphenyl)anthracene with pyrrole, successfully prevented unfavourable quenching due to the aggregation and π-π stacking of highly conjugated anthracene building blocks. The highly extended and conjugated structure enabled AP-CMP with high fluorescence, porosity, and the ability to detect nitrofuran antibiotics selectively and rapidly through fluorescence quenching. AP-CMP had low detection limits of 0.62 ppm for Nitrofurazone (NFZ), 0.67 ppm for nitrofurantoin (NFT), and 0.77 ppm for furazolidone (FZD).
MOF and COF ligands
Aldehyde ligand for cross-linked COF networks
Worldwide shipping
Quick and reliable shipping
High purity
>98% High purity
Facile reactions
Aldehyde possesses excellent reactivity
General Information
CAS Number | 324750-99-4 |
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Chemical Formula | C28H18O2 |
Full Name | 9,10-Bis(4-formylphenyl)anthracene |
Molecular Weight | 386.44 g/mol |
Synonyms | BFPA, 4,4'-(Anthracene-9,10-diyl)dibenzaldehyde |
Classification / Family | Anthracenes, COF ligands |
Chemical Structure
Product Details
Purity | > 98% |
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Melting Point | 295 ºC (lit.) |
Appearance | White to off-white powder/crystals |
MSDS Documentation
9,10-Bis(4-formylphenyl)anthracene MSDS Sheet
Literature and Reviews
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Anthracene and Porphyrin-based Conjugated Microporous Polymer for Nitrofuran Antibiotics and Nitroaromatic Explosives Detection, C. Qi et al., J. Environ. Chem. Eng., 111553 (2023); DOI: 10.1016/j.jece.2023.111553.
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Porphyrin–anthracene covalent organic frameworks for sustainable photosterilization, J. Guo et al., J. Mater. Chem. B, 2023, DOI: 10.1039/D3TB02017G.
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Anthracene-incorporated cyanostilbene based donor–acceptor systems: intramolecular charge transfer and aggregation induced emission, C. Femina et al., New J. Chem., 47, 13810-13819 (2023); DOI: 10.1039/D3NJ00478C.
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Preparation, characterization, pH titration, and electrochemical properties of an anthracene-bridged binuclear ruthenium complex containing imidazole, H. Yin et al., J. Coord. Chem., 72, 2957-2967 (2019); DOI: 10.1080/00958972.2019.1678031.
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Functionality-Dependent Electrical Conductivity in Two-Dimensional Covalent Organic Frameworks, S. Bommakanti et al., J. Phys. Chem. C, 127 (17), 8352–8361 (2023); DOI: 10.1021/acs.jpcc.3c01387.
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High efficiency in blue organic light-emitting diodes using an anthracene-based emitting material, J. Park et al., Thin Solid Films, 516, 2917-2921 (2008); DOI: 10.1016/j.tsf.2007.06.004.
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Exceptional Thermal Stability in a Supramolecular Organic Framework: Porosity and Gas Storage, W. Yang et al., J. Am. Chem. Soc., 132, 41, 14457–14469 (2010); DOI: 10.1021/ja1042935.
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