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Atomfair Methyl 2-(4-methoxy-3-nitrophenyl)acetate C10H11NO5

Description Methyl 2-(4-methoxy-3-nitrophenyl)acetate (CAS No. 34837-88-2) is a high-purity organic compound with the molecular formula C10H11NO5. This ester derivative features a methoxy and nitro functional group on the phenyl ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 225.20 g/mol , it is commonly used in the development of fine chemicals, agrochemicals, and active pharmaceutical ingredients (APIs). Our product is rigorously tested for purity and stability, ensuring optimal performance in sensitive applications. Available in various packaging options, it is ideal for researchers requiring precise and reliable reagents.

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Description

Description

Methyl 2-(4-methoxy-3-nitrophenyl)acetate (CAS No. 34837-88-2) is a high-purity organic compound with the molecular formula C10H11NO5. This ester derivative features a methoxy and nitro functional group on the phenyl ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 225.20 g/mol, it is commonly used in the development of fine chemicals, agrochemicals, and active pharmaceutical ingredients (APIs). Our product is rigorously tested for purity and stability, ensuring optimal performance in sensitive applications. Available in various packaging options, it is ideal for researchers requiring precise and reliable reagents.

  • CAS No: 34837-88-2
  • Molecular Formula: C10H11NO5
  • Molecular Weight: 225.20
  • Exact Mass: 225.06372245
  • Monoisotopic Mass: 225.06372245
  • IUPAC Name: methyl 2-(4-methoxy-3-nitrophenyl)acetate
  • SMILES: COC1=C(C=C(C=C1)CC(=O)OC)[N+](=O)[O-]
  • Synonyms: methyl 2-(4-methoxy-3-nitrophenyl)acetate, 34837-88-2, 4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER, MFCD09754963, CHEMBL453034

Application

Methyl 2-(4-methoxy-3-nitrophenyl)acetate serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. It is utilized in the preparation of nitroaromatic compounds, which are precursors to dyes, fragrances, and bioactive agents. Researchers also employ this ester in coupling reactions and as a building block for heterocyclic chemistry. Its stability and reactivity make it suitable for multi-step synthetic pathways.

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