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Atomfair 5-Bromo-2-nitrobenzotrifluoride C7H3BrF3NO2

Description 5-Bromo-2-nitrobenzotrifluoride (CAS No. 344-38-7) is a high-purity halogenated nitroaromatic compound with the molecular formula C7H3BrF3NO2. This specialized chemical, also known by its IUPAC name 4-bromo-1-nitro-2-(trifluoromethyl)benzene , features a trifluoromethyl group and a nitro group on a brominated benzene ring, making it a versatile intermediate for synthetic organic chemistry and pharmaceutical research. Its unique structure enables applications in cross-coupling reactions, nucleophilic substitutions, and as a building block for agrochemicals or bioactive molecules. Available in >98% purity (GC), this compound is supplied in rigorously tested batches with detailed analytical certificates (COA, MSDS). Store in a cool, dry place under inert atmosphere…

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Description

Description

5-Bromo-2-nitrobenzotrifluoride (CAS No. 344-38-7) is a high-purity halogenated nitroaromatic compound with the molecular formula C7H3BrF3NO2. This specialized chemical, also known by its IUPAC name 4-bromo-1-nitro-2-(trifluoromethyl)benzene, features a trifluoromethyl group and a nitro group on a brominated benzene ring, making it a versatile intermediate for synthetic organic chemistry and pharmaceutical research. Its unique structure enables applications in cross-coupling reactions, nucleophilic substitutions, and as a building block for agrochemicals or bioactive molecules. Available in >98% purity (GC), this compound is supplied in rigorously tested batches with detailed analytical certificates (COA, MSDS). Store in a cool, dry place under inert atmosphere to ensure stability.

  • CAS No: 344-38-7
  • Molecular Formula: C7H3BrF3NO2
  • Molecular Weight: 270.00
  • Exact Mass: 268.92993
  • Monoisotopic Mass: 268.92993
  • IUPAC Name: 4-bromo-1-nitro-2-(trifluoromethyl)benzene
  • SMILES: C1=CC(=C(C=C1Br)C(F)(F)F)[N+](=O)[O-]
  • Synonyms: 5-Bromo-2-nitrobenzotrifluoride, 344-38-7, DTXSID90187970, DTXCID50110461, 670-400-3

Application

5-Bromo-2-nitrobenzotrifluoride serves as a key intermediate in Suzuki-Miyaura and Buchwald-Hartwig cross-coupling reactions for pharmaceutical synthesis. Its electron-deficient aromatic ring facilitates nucleophilic aromatic substitutions in the development of fluorinated agrochemicals. Researchers also utilize it to synthesize trifluoromethyl-substituted dyes and liquid crystal materials.

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