Oxime ethers
Oxime ethers, a class of organic compounds with a unique structure consisting of an oxime group (-N=O) and an ether linkage (C-O-C), are widely recognized for their diverse applications in various chemical industries. These compounds can be synthesized through the reaction between aldehydes or ketones and primary or secondary amines, leading to a mixture of α-oximes and oxime ethers, respectively. Notably, oxime ethers exhibit excellent solubility properties due to the presence of both hydrophobic and hydrophilic groups, making them valuable in organic synthesis as protecting groups for aldehydes and ketones. They are also utilized in pharmaceuticals, agrochemicals, and polymer chemistry for their reactivity and versatility. Furthermore, oxime ethers have potential applications in catalysis and materials science, contributing to the development of new functional materials with enhanced properties through tailored molecular structures.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Acetic acid, (ethoxyimino)- | 88012-60-6 | C4H7NO3 |
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2-Propanone,O-[1-(hydroxymethyl)pentyl]oxime | 5001-44-5 | C9H19NO2 |
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4-tert-butyl-N-methoxycyclohexanimine | 61580-74-3 | C11H21NO |
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2,5-Dimethyl-1,4-benzoquinone; Monoxime, Me ether | 858012-43-8 | C9H11NO2 |
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Propanoic acid, 2-(methoxyimino)- | 27752-38-1 | C4H7NO3 |
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4H-1,2-Oxazine, 5,6-dihydro-3-methyl- | 39703-76-9 | C5H9NO |
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O-Methyloxime Acetaldehyde | 33581-43-0 | C3H7NO |
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Propanoic acid, 2-(ethoxyimino)- | 88012-62-8 | C5H9NO3 |
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methoxy(propan-2-ylidene)amine | 3376-35-0 | C4H9NO |
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Ethanone, 1-(6-ethoxy-5,6-dihydro-4H-1,2-oxazin-3-yl)- | 80322-63-0 | C8H13NO3 |
Related Literature
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Stephen P. Fletcher,Richard B. C. Jagt,Ben L. Feringa Chem. Commun., 2007, 2578-2580
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Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
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Dhamodaran Manikandan,S. Amirthapandian,I. S. Zhidkov,A. I. Kukharenko,S. O. Cholakh,Ramaswamy Murugan Phys. Chem. Chem. Phys., 2018,20, 6500-6514
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Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003
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