Beta-diketones
Beta-diketones are a class of organic compounds characterized by the presence of two ketone groups attached to a common carbon atom, forming a three-membered ring. These molecules exhibit distinctive chemical properties and play significant roles in various applications.
Typically, beta-diketones possess high reactivity due to their polar functional groups and conjugated structure, making them valuable intermediates in organic synthesis. They are often used as chelating agents, capable of forming stable complexes with metal ions through coordination bonds, particularly with transition metals like zinc and titanium. This property finds applications in catalysts for polymerization reactions, coatings, and surface treatments.
Moreover, beta-diketones serve as precursors in the production of advanced materials such as diamond-like carbon films and are also employed in the formulation of fragrances due to their characteristic aroma profiles. Their ability to stabilize metal ions can contribute to environmental applications like water purification processes by facilitating the removal of heavy metals from aqueous solutions.
In summary, beta-diketones represent versatile molecules with a broad range of industrial uses across chemical synthesis, materials science, and environmental technologies.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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12,14-Nonacosanedione | 58141-94-9 | C29H56O2 |
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10,14,16-Hentriacontanetrione | 60368-11-8 | C31H58O3 |
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2,7-Dihydroxy-13-nor-1(10)-nardosinen-11-one; (2α,6α,7α)-form, 7-Ketone | 874384-38-0 | C14H20O3 |
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12,14-tritriacontanedione | 63142-47-2 | C33H64O2 |
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3-acetyl-5-(1-methylpropyl)-2,4-Pyrrolidinedione | 33061-01-7 | C10H15NO3 |
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2,4-Pyrrolidinedione,3-acetyl-5-[(1S)-1-methylpropyl]-, (5S)- | 27778-66-1 | C10H15NO3 |
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14,16-Hentriacontanedione | 24724-84-3 | C31H60O2 |
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1,3,5-Cyclohexanetrione, 2,2,4,4-tetramethyl- | 7181-79-5 | C10H14O3 |
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1,3-Cyclopentanedione,4-octyl- (9CI) | 126624-26-8 | C13H22O2 |
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Cryptocin | 264913-57-7 | C21H31NO4 |
Related Literature
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Xiao Liu,Jun Xu,Yinyun Lv,Wenyu Wu,Weisheng Liu,Yu Tang Dalton Trans., 2013,42, 9840-9846
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Priyambada Nayak,Tanmaya Badapanda,Anil Kumar Singh,Simanchalo Panigrahi RSC Adv., 2017,7, 16319-16331
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Soumaya Khlifi,Gregory Mouille,Jonathan Farjon Anal. Methods, 2017,9, 2328-2333
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Kui Wu,Zhihua Yang,Shilie Pan Dalton Trans., 2015,44, 19856-19864
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