Atomfair Methyl 2-(3-bromophenyl)acetate C9H9BrO2

Description Methyl 2-(3-bromophenyl)acetate (CAS No. 150529-73-0) is a high-purity organic compound with the molecular formula C9H9BrO2. This ester derivative of 3-bromophenylacetic acid is a versatile intermediate widely used in pharmaceutical, agrochemical, and material science research. Its well-defined structure, featuring a bromine substituent at the meta-position of the phenyl ring, makes it a valuable building block for Suzuki coupling reactions and other cross-coupling methodologies. Supplied as a clear to pale-yellow liquid, our product undergoes rigorous QC testing including GC, NMR, and HPLC to ensure ??98% purity. Packaged under inert gas to enhance stability, it is available in quantities ranging from grams…

Description

Description

Methyl 2-(3-bromophenyl)acetate (CAS No. 150529-73-0) is a high-purity organic compound with the molecular formula C9H9BrO2. This ester derivative of 3-bromophenylacetic acid is a versatile intermediate widely used in pharmaceutical, agrochemical, and material science research. Its well-defined structure, featuring a bromine substituent at the meta-position of the phenyl ring, makes it a valuable building block for Suzuki coupling reactions and other cross-coupling methodologies. Supplied as a clear to pale-yellow liquid, our product undergoes rigorous QC testing including GC, NMR, and HPLC to ensure ??98% purity. Packaged under inert gas to enhance stability, it is available in quantities ranging from grams to kilograms to meet both lab-scale and bulk requirements.

  • CAS No: 150529-73-0
  • Molecular Formula: C9H9BrO2
  • Molecular Weight: 229.07
  • Exact Mass: 227.97859
  • Monoisotopic Mass: 227.97859
  • IUPAC Name: methyl 2-(3-bromophenyl)acetate
  • SMILES: COC(=O)CC1=CC(=CC=C1)Br
  • Synonyms: Methyl 2-(3-bromophenyl)acetate, 150529-73-0, Methyl 3-bromophenylacetate, DTXSID40471755, DTXCID50422571

Application

Methyl 2-(3-bromophenyl)acetate serves as a key synthetic intermediate in the preparation of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Researchers utilize its bromine moiety for palladium-catalyzed cross-coupling reactions to construct biaryl systems in drug discovery. The compound also finds application in liquid crystal and polymer additive synthesis, where the ester group allows further functionalization. Its meta-substituted aromatic structure is particularly valuable for studying steric effects in molecular design.

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