Home Chemistry Heterocyclic building blocks Azetidines N-((6r,7r)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-7-yl)-2-phenylacetamide
Hydrolysis: Under acidic or basic conditions, the amide bond (-CONH-) can undergo hydrolysis to yield the corresponding carboxylic acid and amine.
Acylation: The amine group can undergo acylation reactions with acyl chlorides or anhydrides to form amide derivatives.
Ring-opening reactions: The bicyclic ring system (1-azabicyclo[4.2.0]oct-2-en-7-yl) can undergo ring-opening reactions under specific conditions.
Substitution reactions: The phenyl group can undergo various substitution reactions, such as nucleophilic aromatic substitution or electrophilic aromatic substitution, depending on the reagents and conditions.
Cyclization reactions: Depending on the reaction conditions, intramolecular cyclization reactions could occur due to the presence of functional groups.
Condensation reactions: The compound may participate in condensation reactions with suitable reagents, leading to the formation of new compounds.
Isomerization: Depending on the reaction conditions, isomerization reactions of the double bond in the bicyclic ring system may occur.
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