Diazinanes
Diazinanes are a class of heterocyclic organic compounds featuring a five-membered ring with one nitrogen atom and four carbon atoms, often referred to as 1,3-diazines. These molecules play significant roles in various fields including pharmaceuticals, agriculture, and materials science. The unique electronic structure and stability of diazinanes make them attractive for their potential use in drug design, particularly targeting nucleophilic aromatic substitution reactions. Additionally, due to their ability to form metal complexes, they are explored for applications such as catalysts and sensors. The flexibility in functionalization at various positions allows for the development of diverse compounds with tailored properties, making diazinanes a versatile platform for chemical synthesis and biological studies.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Hemibatzelladine J | 1777816-35-9 | C23H40N6O3 |
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Hemibatzelladine J; 19,20Z-Didehydro | 1777816-39-3 | C23H38N6O3 |
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Batzelladine J | 866403-32-9 | C41H67N9O4 |
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Cybastacine A; Δ7-Isomer | 2218478-74-9 | C26H43N3O |
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N/A | 1000415-63-3 | C11H17N3O6 |
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2,5,8-trimethyl-dodecahydro-1,4,7,9b-tetraaza-phenalene | 54352-31-7 | C12H24N4 |
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tetrahydro-2-thioxo-4(1H)-Pyrimidinone | 5366-11-0 | C4H6N2OS |
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1,2-Diazinan-3-one | 19283-07-9 | C4H8N2O |
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2-(tert-butoxy)carbonyl-6-oxo-1,2-diazinane-4-carboxylic acid | 1427380-68-4 | C10H16N2O5 |
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6-phenyl-2-sulfanylidene-1,3-diazinan-4-one | 6300-96-5 | C10H10N2OS |
Related Literature
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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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Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
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Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
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Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
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