Home Chemistry Heterocyclic Building Blocks Pyrrolidines 5-Azaspiro[2.4]Heptane
Nucleophilic Substitution: If there are suitable leaving groups on the molecule, nucleophilic substitution reactions can occur. This might involve the replacement of one functional group with another by nucleophilic attack.
Acid-Base Reactions: Compounds with nitrogen atoms can act as bases, accepting protons (H+
) from acids or donating lone pairs of electrons. The reactivity in acid-base reactions will depend on the basicity of the nitrogen atom.
Ring-Opening Reactions: Spirocyclic compounds can undergo ring-opening reactions when exposed to certain conditions or reagents. This can lead to the formation of open-chain compounds.
Substitution Reactions: Depending on the functional groups attached to the spirocyclic structure, substitution reactions may take place. For instance, if there are halogen atoms present, they can be replaced by other nucleophiles.
Cyclization Reactions: In some cases, 5-azaspiro[2.4]heptane or similar compounds may undergo intramolecular cyclization reactions, forming new ring structures.
Addition Reactions: If the compound contains unsaturated bonds, it may undergo addition reactions, where atoms or groups are added to the double bonds.
Tautomerism: If the compound can exist in multiple tautomeric forms, it may undergo tautomeric shifts, which involve the rearrangement of atoms and bonds within the molecule.
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tert-Butyl (7S)-7-amino-5-azaspiro[2.4]heptane-5-carboxylate
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tert-Butyl 7-amino-5-azaspiro[2.4]heptane-5-carboxylate
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(S)-tert-Butyl 5-azaspiro[2.4]heptan-7-ylcarbamate
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(R)-tert-Butyl 5-azaspiro[2.4]heptan-7-ylcarbamate
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(R)-5-(tert-Butoxycarbonyl)-5-azaspiro[2.4]heptane-6-carboxylic acid
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1,1-Difluoro-5-azaspiro[2.4]heptane hydrochloride
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(3R,6S)-5-(tert-Butoxycarbonyl)-1,1-difluoro-5-azaspiro[2.4]heptane-6-carboxylic acid
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(3S,6S)-5-(tert-Butoxycarbonyl)-1,1-difluoro-5-azaspiro[2.4]heptane-6-carboxylic acid
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Potassium (S)-5-(tert-butoxycarbonyl)-5-azaspiro[2.4]heptane-6-carboxylate
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(S)-5-(tert-Butoxycarbonyl)-5-azaspiro[2.4]heptane-6-carboxylic acid
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5-tert-Butyl 1-ethyl 5-azaspiro[2.4]heptane-1,5-dicarboxylate
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(R)-tert-Butyl 7-amino-5-azaspiro[2.4]heptane-5-carboxylate
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