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Atomfair 2-Bromo-4-methoxy-5-(benzyloxy)benzoic acid C15H13BrO4

Description 2-Bromo-4-methoxy-5-(benzyloxy)benzoic acid (CAS No. 24958-42-7) is a high-purity, synthetic aromatic carboxylic acid derivative designed for advanced research and pharmaceutical applications. With the molecular formula C15H13BrO4, this compound features a brominated benzoic acid core substituted with methoxy and benzyloxy functional groups, offering versatile reactivity for organic synthesis. Its IUPAC name, 2-bromo-4-methoxy-5-phenylmethoxybenzoic acid , reflects its precise structural configuration. Ideal for use as a building block in medicinal chemistry, this compound is rigorously tested for purity and consistency, ensuring reliable performance in coupling reactions, ligand design, and intermediate synthesis. Available in sealed packaging to maintain stability, it is suitable for laboratory…

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Description

Description

2-Bromo-4-methoxy-5-(benzyloxy)benzoic acid (CAS No. 24958-42-7) is a high-purity, synthetic aromatic carboxylic acid derivative designed for advanced research and pharmaceutical applications. With the molecular formula C15H13BrO4, this compound features a brominated benzoic acid core substituted with methoxy and benzyloxy functional groups, offering versatile reactivity for organic synthesis. Its IUPAC name, 2-bromo-4-methoxy-5-phenylmethoxybenzoic acid, reflects its precise structural configuration. Ideal for use as a building block in medicinal chemistry, this compound is rigorously tested for purity and consistency, ensuring reliable performance in coupling reactions, ligand design, and intermediate synthesis. Available in sealed packaging to maintain stability, it is suitable for laboratory use under controlled conditions.

  • CAS No: 24958-42-7
  • Molecular Formula: C15H13BrO4
  • Molecular Weight: 337.16
  • Exact Mass: 335.99972
  • Monoisotopic Mass: 335.99972
  • IUPAC Name: 2-bromo-4-methoxy-5-phenylmethoxybenzoic acid
  • SMILES: COC1=C(C=C(C(=C1)Br)C(=O)O)OCC2=CC=CC=C2
  • Synonyms: 24958-42-7, 2-BROMO-4-METHOXY-5-(BENZYLOXY)BENZOIC ACID, 2-Bromo-4-methoxy-5-benzyloxybenzoic acid, 5-Benzyloxy-2-bromo-4-methoxybenzoic Acid, 2-bromo-5-benzyloxy-4-methoxybenzoic acid

Application

2-Bromo-4-methoxy-5-(benzyloxy)benzoic acid serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical research. Its reactive bromo and carboxylic acid groups enable participation in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to construct biaryl scaffolds. The benzyloxy and methoxy substituents enhance solubility and direct further functionalization, making it valuable for developing drug candidates or agrochemicals. Researchers also utilize it in studying enzyme inhibition or as a precursor for fluorescent probes.

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