Home Chemistry Heterocyclic Building Blocks Aliphatic Heterocycles 11,12-Didehydro-5,6-Dihydrodibenz[B,F]Azocine
Hydrogenation: The double bonds in the molecule can be reduced to saturated bonds using hydrogenation. This can be done catalytically using a metal catalyst (e.g., palladium on carbon) and hydrogen gas.
Halogenation: You can react the compound with halogens (e.g., chlorine or bromine) to add halogen atoms to the aromatic rings or other reactive sites in the molecule.
Acylation: Treatment with acyl chlorides or anhydrides can lead to acylation of suitable functional groups (e.g., amine groups), forming amides.
Nucleophilic Substitution: If there are suitable leaving groups (e.g., halogens) on the molecule, nucleophilic substitution reactions can occur.
Grignard Reaction: The compound can react with Grignard reagents (organomagnesium compounds) to form new carbon-carbon bonds and introduce various functional groups.
Oxidation/Reduction: Depending on the conditions, you can selectively oxidize or reduce specific functional groups in the molecule.
Ring-opening reactions: If the molecule contains strained or reactive rings, ring-opening reactions can occur under appropriate conditions.
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N-[3-(11,12-Didehydrodibenz[b,f]azocin-5(6H)-yl)-3-oxopropyl]-2,2,2-trifluoroacetamide
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N-[3-(11,12-Didehydrodibenz[b,f]azocin-5(6H)-yl)-3-oxopropyl]urea
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1-(11,12-Didehydrodibenz[b,f]azocin-5(6H)-yl)ethanone
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