Home Chemistry Heterocyclic Building Blocks Piperidines Piperidin-3-Ylmethanamine
Nucleophilic substitution: The amino group can act as a nucleophile in substitution reactions, displacing other functional groups such as halides or leaving groups.
Acylation: The nitrogen atom can undergo acylation reactions, where an acyl group is introduced onto the nitrogen atom, forming an amide.
Reductive amination: It can undergo reductive amination reactions, where the amino group reacts with a carbonyl compound in the presence of a reducing agent to form secondary or tertiary amines.
Alkylation: The nitrogen atom can undergo alkylation reactions, where an alkyl group is introduced onto the nitrogen atom.
Ring-opening reactions: The piperidine ring can undergo ring-opening reactions under certain conditions, leading to the formation of open-chain compounds.
Oxidation: The amine group can be oxidized to form corresponding amine oxides or imines.
Reduction: The compound can undergo reduction reactions, where functional groups like nitro groups or carbonyl groups can be reduced to their respective amines or alcohols.
Cyclization reactions: Under specific conditions, the compound can undergo cyclization reactions to form cyclic compounds with different ring sizes.
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tert-Butyl 3-(aminomethyl)piperidine-1-carboxylate
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tert-Butyl (S)-3-(aminomethyl)piperidine-1-carboxylate
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(S)-tert-Butyl 3-(aminomethyl)piperidine-1-carboxylate hydrochloride
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