Phthalazines
Phthalazines are a class of heterocyclic aromatic compounds characterized by the presence of a benzene ring fused to an imidazole ring. This structure results in unique electronic and chemical properties, making phthalazines valuable in various applications across multiple industries.
Phthalazines exhibit significant photochemical and photophysical behavior due to their conjugated system, which can be exploited in fields such as organic solar cells, light-emitting diodes (LEDs), and sensors. In addition, these compounds possess potential biological activities, including antiviral, antibacterial, and anticancer properties. They are also utilized in the pharmaceutical industry for drug development, acting as precursors or intermediates.
The versatile nature of phthalazines allows them to be modified through various synthetic routes, enabling the creation of derivatives with specific functional groups tailored to meet the demands of different applications. Their ability to form stable complexes with metal ions further expands their utility in coordination chemistry and catalysis.
Overall, phthalazines represent a diverse and intriguing class of compounds that continue to attract significant research interest due to their unique properties and potential applications in both fundamental science and industrial settings.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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1,4-Phthalazinedione, 2,3-dihydro-2-methyl-3-phenyl- | 89811-41-6 | C15H12N2O2 |
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4-Nitrophthalhydrazide | 3682-19-7 | C8H5N3O4 |
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N-(4-Aminobutyl)-N-ethylisoluminol | 66612-29-1 | C14H20N4O2 |
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4-chlorophthalazin-1-amine | 13580-86-4 | C8H6ClN3 |
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1,2,3,4-Tetrahydrophthalazine | 13152-89-1 | C8H10N2 |
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(S)-Azelastine Hydrochloride | 153408-27-6 | C22H25Cl2N3O |
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7-Bromo-phthalazin-1-ol | 152265-57-1 | C8H5BrN2O |
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4-(4-Chlorophenyl)methyl-1(2H)-phthalazinone | 53242-88-9 | C15H11ClN2O |
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1,4-Phthalazinedione,5-amino- | 60851-83-4 | C8H5N3O2 |
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1(2H)-Phthalazinone,4-(2-hydroxyethoxy)- | 69776-14-3 | C10H10N2O3 |
Related Literature
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
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Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
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Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
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Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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