Enamines
Enamines are a class of organic compounds characterized by the presence of an imine derived from an amine, typically involving a carbon-nitrogen double bond adjacent to a carbonyl group. These compounds have unique reactivity and structural flexibility, making them versatile in synthetic chemistry. Enamines can be prepared via various methods including aldehyde or ketone reduction with organolithiums, Grignard reagents, or other nucleophiles. Due to their ability to undergo a variety of reactions such as conjugate addition, Alder-Devine reaction, and Michael additions, enamines serve as valuable intermediates in the synthesis of diverse organic molecules. Their use extends across pharmaceuticals, agrochemicals, and fine chemicals where they are often employed for constructing complex molecular frameworks efficiently.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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5-Methyl-1-cyclohepten-1-amine | 53907-56-5 | C8H15N |
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tert-butyl(prop-1-en-1-yl)amine | 1314991-39-3 | C7H15N |
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N-ethenylcyclopropanamine | 2092438-47-4 | C5H9N |
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2-aminocyclopent-1-ene-1-carbodithioic acid | 20735-33-5 | C6H9NS2 |
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Ethenamine (9CI) | 593-67-9 | C2H5N |
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1-Cyclopentene-1-carbodithioicacid, 2-(methylamino)- | 34281-24-8 | C7H11NS2 |
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(2-methylprop-1-en-1-yl)(2-methylpropyl)amine | 65500-37-0 | C8H17N |
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