Home Chemistry Heterocyclic Building Blocks Isoquinolines 1H-Benzo[De]Isoquinoline-1,3(2H)-Dione
Aromatic Substitution: The compound contains an aromatic ring, so it can undergo electrophilic aromatic substitution reactions. For example, you can introduce various substituents or functional groups onto the aromatic ring through reactions like Friedel-Crafts acylation or alkylation.
Reduction: 1H-benzo[de]isoquinoline-1,3(2H)-dione can be reduced using reducing agents like lithium aluminum hydride (LiAlH4) to produce the corresponding dihydro compound.
Oxidation: Oxidation reactions can convert the compound into its oxidized forms, such as quinones. Common oxidizing agents like potassium permanganate (KMnO4) can be used for this purpose.
Ring-Opening Reactions: Depending on the reaction conditions, you can perform ring-opening reactions to break the cyclic structure. For instance, using strong bases like sodium or potassium hydroxide can lead to ring-opening reactions.
Nucleophilic Addition: The carbonyl group in the compound can undergo nucleophilic addition reactions. For example, it can react with amines to form imine derivatives.
Hydrolysis: The compound can undergo hydrolysis reactions under acidic or basic conditions, leading to the cleavage of the dione ring and the formation of different products.
Condensation Reactions: It can participate in condensation reactions with various reagents to form larger and more complex molecules.
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6-Bromo-1H-benzo[de]isoquinoline-1,3(2H)-dione
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6-Bromo-2-(2-hydroxyethyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione
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2-(2-Aminoethyl)-6-(dimethylamino)-1H-benz[de]isoquinoline-1,3(2H)-dione
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6-Bromo-2-(2-ethylhexyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione
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6-(6-(Dimethylamino)-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)hexanoic acid
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1,3-Dioxo-1H-benzo[de]isoquinolin-2(3H)-yl trifluoromethanesulfonate
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