N-substituted carboxylic acid imides
N-Substituted Carboxylic Acid Imides are a diverse class of organic compounds characterized by the presence of an imide functional group attached to a carboxylate moiety. These molecules find applications in various fields due to their unique properties and reactivity. They can serve as intermediates in pharmaceuticals, where they often act as precursors for drug synthesis. In materials science, N-substituted carboxylic acid imides are used to develop functional polymers with enhanced mechanical properties and thermal stability. These compounds also play a significant role in the formulation of environmentally friendly coatings due to their ability to form hydrophobic layers upon polymerization. Additionally, they have potential applications in catalysis, acting as Lewis acids or Bronsted acids depending on the substituents attached to the imide group. The versatile nature of these molecules allows for extensive modification and optimization tailored to specific application needs.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2H-Pyrrol-2-one,1-[(2R,3R)-3-[(aminocarbonyl)oxy]-8,8,9,9-tetrachloro-2-methyl-1-oxodecyl]-1,5-dihydro-4-methoxy-5-methyl-,(5S)- | 159903-50-1 | C18H26Cl4N2O5 |
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Jamaicamide A | 373641-52-2 | C27H36BrClN2O4 |
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Jamaicamide A; Debromo, 19,20-dihydro | 757964-07-1 | C27H39ClN2O4 |
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Pukeleimid E | 72362-21-1 | C13H14N2O4 |
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2H-Pyrrol-2-one,1-acetyl-1,5-dihydro-4-methoxy- | 96909-02-3 | C7H9NO3 |
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(+)-Dysidine | 95272-90-5 | C16H22Cl3NO4 |
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Pukeleimid D | 72362-20-0 | C13H16N2O6 |
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Pukeleimide G | 72362-23-3 | C14H16N2O5 |
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PYRROLO[3,4-D]IMIDAZOLE-4,6(1H,5H)-DIONE, 5-(3-METHYL-2-BUTENYL)- | 643751-34-2 | C10H11N3O2 |
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Jamaicamide B | 757964-06-0 | C27H37ClN2O4 |
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