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Atomfair Methyl 2-(3-oxocyclobutyl)acetate C7H10O3

Description Methyl 2-(3-oxocyclobutyl)acetate (CAS No. 1148152-49-1) is a high-purity cyclic ketone ester with the molecular formula C7H10O3. This compound, also known by its IUPAC name methyl 2-(3-oxocyclobutyl)acetate , is a versatile intermediate in organic synthesis and pharmaceutical research. Its unique cyclobutyl ketone structure makes it valuable for constructing complex molecular frameworks. Available in various quantities, this product is rigorously tested to ensure ??95% purity (GC) and is supplied in sealed containers under inert atmosphere to maintain stability. Key identifiers include EC 839-571-3 and MDL number MFCD20134006.

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Description

Description

Methyl 2-(3-oxocyclobutyl)acetate (CAS No. 1148152-49-1) is a high-purity cyclic ketone ester with the molecular formula C7H10O3. This compound, also known by its IUPAC name methyl 2-(3-oxocyclobutyl)acetate, is a versatile intermediate in organic synthesis and pharmaceutical research. Its unique cyclobutyl ketone structure makes it valuable for constructing complex molecular frameworks. Available in various quantities, this product is rigorously tested to ensure ??95% purity (GC) and is supplied in sealed containers under inert atmosphere to maintain stability. Key identifiers include EC 839-571-3 and MDL number MFCD20134006.

  • CAS No: 1148152-49-1
  • Molecular Formula: C7H10O3
  • Molecular Weight: 142.15
  • Exact Mass: 142.062994177
  • Monoisotopic Mass: 142.062994177
  • IUPAC Name: methyl 2-(3-oxocyclobutyl)acetate
  • SMILES: COC(=O)CC1CC(=O)C1
  • Synonyms: Methyl 2-(3-oxocyclobutyl)acetate, 839-571-3, 1148130-30-6, Cyclobutaneacetic acid, 3-oxo-, methyl ester, MFCD20134006

Application

Methyl 2-(3-oxocyclobutyl)acetate serves as a key building block in medicinal chemistry for the synthesis of cyclobutane-containing drug candidates. The strained cyclobutane ring system is valuable in fragment-based drug discovery. Researchers utilize this compound as a precursor for [2+2] cycloaddition reactions to create complex spirocyclic architectures. Its reactive ketone and ester functionalities enable diverse derivatization pathways.

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