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Atomfair Methyl 3-bromo-2-hydroxybenzoate C8H7BrO3

Description Methyl 3-bromo-2-hydroxybenzoate (CAS No. 28165-45-9) is a high-purity organic compound with the molecular formula C8H7BrO3. This aromatic ester features a bromo and hydroxyl functional group adjacent to the ester moiety, making it a versatile intermediate for synthetic organic chemistry and pharmaceutical research. Its precise structure, methyl 3-bromo-2-hydroxybenzoate , ensures excellent reactivity in electrophilic substitutions and coupling reactions. Ideal for researchers, this compound is rigorously tested for purity (typically ??95% by HPLC or GC) and is supplied in sealed packaging under inert conditions to ensure stability. Suitable for lab-scale experiments, process development, and as a building block for complex molecules.

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Description

Description

Methyl 3-bromo-2-hydroxybenzoate (CAS No. 28165-45-9) is a high-purity organic compound with the molecular formula C8H7BrO3. This aromatic ester features a bromo and hydroxyl functional group adjacent to the ester moiety, making it a versatile intermediate for synthetic organic chemistry and pharmaceutical research. Its precise structure, methyl 3-bromo-2-hydroxybenzoate, ensures excellent reactivity in electrophilic substitutions and coupling reactions. Ideal for researchers, this compound is rigorously tested for purity (typically ??95% by HPLC or GC) and is supplied in sealed packaging under inert conditions to ensure stability. Suitable for lab-scale experiments, process development, and as a building block for complex molecules.

  • CAS No: 28165-45-9
  • Molecular Formula: C8H7BrO3
  • Molecular Weight: 231.04
  • Exact Mass: 229.95786
  • Monoisotopic Mass: 229.95786
  • IUPAC Name: methyl 3-bromo-2-hydroxybenzoate
  • SMILES: COC(=O)C1=C(C(=CC=C1)Br)O
  • Synonyms: Methyl 3-bromo-2-hydroxybenzoate, 28165-45-9, DTXSID90706842, DTXCID20657590, Methyl3-bromo-2-hydroxybenzoate

Application

Methyl 3-bromo-2-hydroxybenzoate is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its reactive bromo and hydroxyl groups facilitate cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, for constructing biaryl systems. Researchers also employ it in the development of anti-inflammatory and antimicrobial agents due to its salicylate-like structure. Additionally, it serves as a precursor for dyes and functional materials in material science.

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