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Atomfair 2,4-Dibromo-6-nitrophenol C6H3Br2NO3

Description 2,4-Dibromo-6-nitrophenol (CAS No. 15969-09-2) is a high-purity brominated nitrophenol compound with the molecular formula C6H3Br2NO3. This halogenated aromatic derivative is characterized by its two bromine substituents at the 2- and 4-positions and a nitro group at the 6-position of the phenolic ring. The compound is supplied as a crystalline solid with exceptional purity (>98%) suitable for advanced organic synthesis, pharmaceutical research, and material science applications. Its unique electronic and steric properties make it valuable as a building block for complex molecular architectures, ligand design, and functional materials. Proper handling under inert atmosphere is recommended due to potential sensitivity to…

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Description

Description

2,4-Dibromo-6-nitrophenol (CAS No. 15969-09-2) is a high-purity brominated nitrophenol compound with the molecular formula C6H3Br2NO3. This halogenated aromatic derivative is characterized by its two bromine substituents at the 2- and 4-positions and a nitro group at the 6-position of the phenolic ring. The compound is supplied as a crystalline solid with exceptional purity (>98%) suitable for advanced organic synthesis, pharmaceutical research, and material science applications. Its unique electronic and steric properties make it valuable as a building block for complex molecular architectures, ligand design, and functional materials. Proper handling under inert atmosphere is recommended due to potential sensitivity to light and moisture.

  • CAS No: 15969-09-2
  • Molecular Formula: C6H3Br2NO3
  • Molecular Weight: 296.90
  • Exact Mass: 296.84592
  • Monoisotopic Mass: 294.84797
  • IUPAC Name: 2,4-dibromo-6-nitrophenol
  • SMILES: C1=C(C=C(C(=C1[N+](=O)[O-])O)Br)Br
  • Synonyms: 2,4-dibromo-6-nitrophenol, 15969-09-2, Phenol, 2,4-dibromo-6-nitro-, 4,6-Dibromo-2-nitrophenol, 26JN516TAT

Application

2,4-Dibromo-6-nitrophenol serves as a versatile intermediate in organic synthesis, particularly for constructing brominated phenolic scaffolds in pharmaceutical development. Researchers utilize its electron-withdrawing groups for selective cross-coupling reactions in catalyst design and materials chemistry. The compound has shown utility in synthesizing antimicrobial agents and flame retardant additives due to its halogen-rich structure.

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