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Atomfair 3-Bromo-5-(ethoxycarbonyl)benzoic acid C10H9BrO4

Description 3-Bromo-5-(ethoxycarbonyl)benzoic acid (CAS No. 2089325-52-8) is a high-purity organic compound with the molecular formula C10H9BrO4, widely utilized in pharmaceutical and chemical research. This benzoic acid derivative features both a bromo substituent and an ethoxycarbonyl group, making it a versatile intermediate for synthesizing complex molecules. Its IUPAC name, 3-bromo-5-ethoxycarbonylbenzoic acid , reflects its precise structural configuration. Ideal for coupling reactions, esterifications, and other functional group transformations, this compound is supplied with rigorous quality control to ensure consistency in reactivity and purity. Suitable for laboratory-scale experiments and industrial applications, it is stored under recommended conditions to maintain stability.

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Description

Description

3-Bromo-5-(ethoxycarbonyl)benzoic acid (CAS No. 2089325-52-8) is a high-purity organic compound with the molecular formula C10H9BrO4, widely utilized in pharmaceutical and chemical research. This benzoic acid derivative features both a bromo substituent and an ethoxycarbonyl group, making it a versatile intermediate for synthesizing complex molecules. Its IUPAC name, 3-bromo-5-ethoxycarbonylbenzoic acid, reflects its precise structural configuration. Ideal for coupling reactions, esterifications, and other functional group transformations, this compound is supplied with rigorous quality control to ensure consistency in reactivity and purity. Suitable for laboratory-scale experiments and industrial applications, it is stored under recommended conditions to maintain stability.

  • CAS No: 2089325-52-8
  • Molecular Formula: C10H9BrO4
  • Molecular Weight: 273.08
  • Exact Mass: 271.96842
  • Monoisotopic Mass: 271.96842
  • IUPAC Name: 3-bromo-5-ethoxycarbonylbenzoic acid
  • SMILES: CCOC(=O)C1=CC(=CC(=C1)C(=O)O)Br
  • Synonyms: 3-Bromo-5-(ethoxycarbonyl)benzoic acid, 2089325-52-8, 3-Bromo-5-(ethoxycarbonyl)benzoicacid, SCHEMBL1928502, 3-bromo-5-ethoxycarbonylbenzoic acid

Application

3-Bromo-5-(ethoxycarbonyl)benzoic acid is primarily employed as a key intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its reactive bromo and carboxyl groups facilitate cross-coupling reactions, such as Suzuki or Heck reactions, for constructing biaryl systems. Researchers also utilize it in esterification processes to modify solubility or bioavailability of target compounds. This compound is valuable in medicinal chemistry for probing structure-activity relationships (SAR) in drug discovery.

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