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.

Properties

• CAS Number: 24958-42-7
• Complexity: 317
• IUPAC Name: 5-benzyloxy-2-bromo-4-methoxy-benzoic acid
• InChI: InChI=1S/C15H13BrO4/c1-19-13-8-12(16)11(15(17)18)7-14(13)20-9-10-5-3-2-4-6-10/h2-8H,9H2,1H3,(H,17,18)
• InChI Key: FBTDEMXQQIWHKX-UHFFFAOYSA-N
• Exact Mass: 335.99972
• Molecular Formula: C15H13BrO4
• Molecular Weight: 337.16
• SMILES: COC1=C(C=C(C(=C1)Br)C(=O)O)OCC2=CC=CC=C2
• Topological: 55.8
• Monoisotopic Mass: 335.99972
• 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, Benzoic acid, 2-bromo-4-methoxy-5-(phenylmethoxy)-, 5-(benzyloxy)-2-bromo-4-methoxybenzoic acid, 2-bromo-4-methoxy-5-phenylmethoxybenzoic acid, 5-Benzyloxy-2-bromo-p-anisic Acid, MFCD03695499, 2-Bromo-4-methoxy-5-(benzyloxy)benzoicacid, SCHEMBL2158619, DTXSID90453627, AKOS015889639, AS-68412, DB-006003, B3332, CS-0450331, T70647

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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