Home Chemistry Heterocyclic Building Blocks Piperidines 6-Azaspiro[2.5]Octane
Nucleophilic Substitution Reactions: Since the compound contains a nitrogen atom, it can undergo nucleophilic substitution reactions. For example, it can react with electrophiles, such as alkyl halides, to replace one of the hydrogen atoms with an alkyl group.
Acid-Base Reactions: Like many amines, 6-azaspiro[2.5]octane can act as a base and undergo acid-base reactions. It can protonate to form its conjugate acid when exposed to strong acids.
Oxidation Reactions: The nitrogen atom in the compound can be oxidized to various oxidation states depending on the conditions. For example, it can be oxidized to form N-oxides or other nitrogen-containing functional groups.
Ring-Opening Reactions: The spirocyclic ring in 6-azaspiro[2.5]octane can potentially undergo ring-opening reactions under certain conditions, leading to the formation of open-chain compounds.
Complexation Reactions: The compound may form complexes with metal ions or other molecules, depending on its chemical environment.
Reduction Reactions: The compound can potentially undergo reduction reactions, where the nitrogen atom is reduced to a lower oxidation state.
Substitution Reactions: 6-azaspiro[2.5]octane can participate in various substitution reactions where one functional group is replaced by another.
Halogenation: Under specific conditions, it might undergo halogenation reactions, where hydrogen atoms on the ring are replaced by halogen atoms.
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Ethyl 6-azaspiro[2.5]octane-1-carboxylate hydrochloride
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tert-Butyl 1-amino-6-azaspiro[2.5]octane-6-carboxylate hydrochloride
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6-[(tert-Butoxy)carbonyl]-6-azaspiro[2.5]octane-5-carboxylic acid
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tert-Butyl (6-azaspiro[2.5]octan-1-yl)carbamate hydrochloride
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(S)-6-(tert-Butoxycarbonyl)-6-azaspiro[2.5]octane-5-carboxylic acid
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6-(tert-Butoxycarbonyl)-6-azaspiro[2.5]octane-1-carboxylic acid
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6-tert-Butyl 1-ethyl 6-azaspiro[2.5]octane-1,6-dicarboxylate
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6-Azaspiro[2.5]octane-1-carboxylic acid hydrochloride
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