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Atomfair 2-Bromo-3-hydroxybenzaldehyde C7H5BrO2

Description 2-Bromo-3-hydroxybenzaldehyde (CAS No. 196081-71-7) is a high-purity aromatic aldehyde compound with the molecular formula C7H5BrO2. This specialized chemical features a bromo substituent at the 2-position and a hydroxyl group at the 3-position of the benzaldehyde ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. The compound is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency in quality and performance. Ideal for use in cross-coupling reactions, heterocyclic synthesis, and as a building block for bioactive molecules. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability.

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Description

Description

2-Bromo-3-hydroxybenzaldehyde (CAS No. 196081-71-7) is a high-purity aromatic aldehyde compound with the molecular formula C7H5BrO2. This specialized chemical features a bromo substituent at the 2-position and a hydroxyl group at the 3-position of the benzaldehyde ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. The compound is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency in quality and performance. Ideal for use in cross-coupling reactions, heterocyclic synthesis, and as a building block for bioactive molecules. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability.

  • CAS No: 196081-71-7
  • Molecular Formula: C7H5BrO2
  • Molecular Weight: 201.02
  • Exact Mass: 199.94729
  • Monoisotopic Mass: 199.94729
  • IUPAC Name: 2-bromo-3-hydroxybenzaldehyde
  • SMILES: C1=CC(=C(C(=C1)O)Br)C=O
  • Synonyms: 2-Bromo-3-hydroxybenzaldehyde, 196081-71-7, Benzaldehyde, 2-bromo-3-hydroxy-, D9D2GQC4CZ, DTXSID30395411

Application

2-Bromo-3-hydroxybenzaldehyde serves as a key precursor in the synthesis of pharmaceutical intermediates, particularly for antimicrobial and anti-inflammatory agents. Its reactive aldehyde and hydroxyl groups enable facile functionalization in palladium-catalyzed coupling reactions. Researchers also utilize this compound in the development of fluorescent probes and coordination complexes for material science applications.

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