Ketimines
Ketimines, also known as iminoketones, are a class of organic compounds characterized by the presence of both an amine and a ketone group in the molecule. These functional groups typically attach to a single carbon atom, forming a unique structural motif that is crucial for their diverse applications. Ketimines can be synthesized through various methods, including reductive amination or condensation reactions between aldehydes/ketones and amines. Due to their potential as precursors in organic synthesis, they are widely used in the preparation of heterocyclic compounds, pharmaceuticals, and materials science. Their ability to undergo ring formation and deamination reactions makes them valuable intermediates for developing complex molecules with specific functional properties. In addition, ketimines have been explored for their catalytic potential, particularly in asymmetric hydrogenation and reduction processes, highlighting their importance in modern chemical research and industry.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Methanamine, N-cyclohexylidene- | 6407-35-8 | C7H13N |
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Cyclohexanimine, 2,2,6,6-tetramethyl- | 64273-89-8 | C10H19N |
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8-Azabicyclo[5.1.0]oct-7-ene | 97704-65-9 | C7H11N |
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Pyrazine,2,3-dihydro-5-methyl-6-(2-methylpropyl)- | 15986-97-7 | C9H16N2 |
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Pyrazine, 5-ethenyl-2,3-dihydro-2,6-dimethyl- | 649563-98-4 | C8H12N2 |
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Methanaminium, N-(4-imino-2,5-cyclohexadien-1-ylidene)-N-methyl- | 33624-86-1 | C8H11N2 |
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Cyclopentanecarbonitrile,2-imino- | 2321-76-8 | C6H8N2 |
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2H-1,4-Diazepine,3,6-dihydro-5,7-dimethyl-, hydrochloride (1:1) | 16418-18-1 | C7H13ClN2 |
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Methyl 2-((tert-butoxycarbonyl)imino)-3,3,3-trifluoropropanoate | 126535-89-5 | C9H12F3NO4 |
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| 51802-55-2 | C9H8N4 |
Related Literature
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