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Atomfair Methyl 2-(2,4-dimethoxyphenyl)acetate C11H14O4

Description Methyl 2-(2,4-dimethoxyphenyl)acetate (CAS No. 55954-25-1) is a high-purity organic ester with the molecular formula C11H14O4. This compound is characterized by its aromatic dimethoxy-substituted phenyl ring coupled with an acetate ester functional group, making it a valuable intermediate in synthetic organic chemistry. With a molecular weight of 210.23 g/mol, it is commonly utilized in pharmaceutical research, agrochemical synthesis, and material science applications. The product is supplied as a clear to pale-yellow liquid with >95% purity (GC), ensuring consistency for sensitive reactions. Proper storage under inert conditions at 2-8??C is recommended to maintain stability.

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Description

Description

Methyl 2-(2,4-dimethoxyphenyl)acetate (CAS No. 55954-25-1) is a high-purity organic ester with the molecular formula C11H14O4. This compound is characterized by its aromatic dimethoxy-substituted phenyl ring coupled with an acetate ester functional group, making it a valuable intermediate in synthetic organic chemistry. With a molecular weight of 210.23 g/mol, it is commonly utilized in pharmaceutical research, agrochemical synthesis, and material science applications. The product is supplied as a clear to pale-yellow liquid with >95% purity (GC), ensuring consistency for sensitive reactions. Proper storage under inert conditions at 2-8??C is recommended to maintain stability.

  • CAS No: 55954-25-1
  • Molecular Formula: C11H14O4
  • Molecular Weight: 210.23
  • Exact Mass: 210.08920892
  • Monoisotopic Mass: 210.08920892
  • IUPAC Name: methyl 2-(2,4-dimethoxyphenyl)acetate
  • SMILES: COC1=CC(=C(C=C1)CC(=O)OC)OC
  • Synonyms: Methyl 2-(2,4-dimethoxyphenyl)acetate, 55954-25-1, DTXSID90472853, DTXCID30423667, 2,4-DIMETHOXY-BENZENEACETIC ACID METHYL ESTER

Application

Methyl 2-(2,4-dimethoxyphenyl)acetate serves as a key building block in the synthesis of complex molecules, particularly in pharmaceutical development where its dimethoxy aromatic structure is leveraged for drug scaffold construction. It is employed in palladium-catalyzed cross-coupling reactions and as a precursor for bioactive compounds targeting neurological and inflammatory pathways. Researchers also utilize this ester in fragrance synthesis due to its aromatic properties.

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