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Atomfair 5-Bromo-2-chloronitrobenzene C6H3BrClNO2

Description 5-Bromo-2-chloronitrobenzene (CAS No. 1189513-50-5) is a high-purity aromatic compound with the molecular formula C6H3BrClNO2and IUPAC name 4-bromo-1-chloro-2-nitrobenzene . This halogenated nitrobenzene derivative is a versatile intermediate in organic synthesis, characterized by its pale yellow to off-white crystalline appearance. With a molecular weight of 236.45 g/mol, it is soluble in common organic solvents such as ethanol, acetone, and dichloromethane but exhibits limited solubility in water. The compound is rigorously tested via GC/HPLC to ensure ??98% purity, making it ideal for research and industrial applications. Proper storage conditions (2-8??C in a tightly sealed container under inert atmosphere) are recommended to maintain…

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Description

Description

5-Bromo-2-chloronitrobenzene (CAS No. 1189513-50-5) is a high-purity aromatic compound with the molecular formula C6H3BrClNO2 and IUPAC name 4-bromo-1-chloro-2-nitrobenzene. This halogenated nitrobenzene derivative is a versatile intermediate in organic synthesis, characterized by its pale yellow to off-white crystalline appearance. With a molecular weight of 236.45 g/mol, it is soluble in common organic solvents such as ethanol, acetone, and dichloromethane but exhibits limited solubility in water. The compound is rigorously tested via GC/HPLC to ensure ??98% purity, making it ideal for research and industrial applications. Proper storage conditions (2-8??C in a tightly sealed container under inert atmosphere) are recommended to maintain stability.

  • CAS No: 1189513-50-5
  • Molecular Formula: C6H3BrClNO2
  • Molecular Weight: 236.45
  • Exact Mass: 234.90357
  • Monoisotopic Mass: 234.90357
  • IUPAC Name: 4-bromo-1-chloro-2-nitrobenzene
  • SMILES: C1=CC(=C(C=C1Br)[N+](=O)[O-])Cl
  • Synonyms: 5-Bromo-2-chloronitrobenzene, 16588-24-2, 4-bromo-1-chloro-2-nitrobenzene, DTXSID80355888, DTXCID90306947

Application

5-Bromo-2-chloronitrobenzene serves as a key precursor in the synthesis of pharmaceuticals, agrochemicals, and specialty dyes. Its reactive nitro and halogen groups enable nucleophilic substitution reactions for constructing complex heterocycles. Researchers utilize this compound in Suzuki-Miyaura coupling reactions to create biphenyl derivatives. It is also employed in the development of liquid crystal materials and corrosion inhibitors.

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