Home Chemistry Organic Building Blocks Amines Benzyl-3-Aminopiperidine-1-Carboxylate
Ester Hydrolysis: Benzyl-3-aminopiperidine-1-carboxylate contains an ester functional group, andesterscan undergo hydrolysis reactions under acidic or basic conditions to produce carboxylic acids and the corresponding alcohols.The amine group in this compound may also participate in the reaction.
Nucleophilic Addition: The amine group can act as a nucleophile and participate in reactions with electrophiles, such as alkyl halides, to form substituted amines through nucleophilic addition reactions.
Amidation Reactions: The amine group can also participate in amidation reactions, where it can react with acyl chlorides, acid anhydrides, or carboxylic acids to form amide bonds.
Reductive Amination: The amine group can undergo reductive amination reactions, where it reacts with a carbonyl compound (e.g., aldehyde or ketone) in the presence of a reducing agent to form secondary or tertiary amines.
Esterification: The carboxylate group can participate in esterification reactions with alcohols to form ester compounds.
Oxidation Reactions: The benzylic carbon in the benzyl group is susceptible to oxidation under certain conditions, leading to the formation of carboxylic acids.
Decarboxylation: The carboxylate group may undergo decarboxylation reactions under specific conditions, leading to the removal of the carboxyl group.
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Benzyl 3-aminopiperidine-1-carboxylate hydrochloride
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(S)-Benzyl 3-aminopiperidine-1-carboxylate hydrochloride
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(S)-Benzyl 3-aminopiperidine-1-carboxylate
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(2R,3R)-Benzyl 3-amino-2-methylpiperidine-1-carboxylate
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Benzyl 3-amino-4,4-difluoropiperidine-1-carboxylate
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