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Atomfair 4-Bromo-2-(trifluoromethoxy)iodobenzene C7H3BrF3IO

Description 4-Bromo-2-(trifluoromethoxy)iodobenzene (CAS No. 175278-12-3) is a high-purity halogenated aromatic compound with the molecular formula C7H3BrF3IO . This specialized chemical features a benzene ring substituted with bromo, iodo, and trifluoromethoxy functional groups, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. Its unique structure enables precise reactivity in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings. Supplied as a crystalline solid with ??98% purity (HPLC), it is rigorously tested for consistency and stability. Ideal for researchers developing fluorinated compounds, agrochemicals, or bioactive molecules. Store under inert conditions at 2-8??C to maintain integrity.

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Description

Description

4-Bromo-2-(trifluoromethoxy)iodobenzene (CAS No. 175278-12-3) is a high-purity halogenated aromatic compound with the molecular formula C7H3BrF3IO. This specialized chemical features a benzene ring substituted with bromo, iodo, and trifluoromethoxy functional groups, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. Its unique structure enables precise reactivity in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings. Supplied as a crystalline solid with ??98% purity (HPLC), it is rigorously tested for consistency and stability. Ideal for researchers developing fluorinated compounds, agrochemicals, or bioactive molecules. Store under inert conditions at 2-8??C to maintain integrity.

  • CAS No: 175278-12-3
  • Molecular Formula: C7H3BrF3IO
  • Molecular Weight: 366.90
  • Exact Mass: 365.83641
  • Monoisotopic Mass: 365.83641
  • IUPAC Name: 4-bromo-1-iodo-2-(trifluoromethoxy)benzene
  • SMILES: C1=CC(=C(C=C1Br)OC(F)(F)F)I
  • Synonyms: 4-Bromo-2-(trifluoromethoxy)iodobenzene, 175278-12-3, DTXSID30371351, DTXCID50322385, 670-910-6

Application

4-Bromo-2-(trifluoromethoxy)iodobenzene serves as a versatile building block in medicinal chemistry for introducing trifluoromethoxy and halogen motifs into drug candidates. It is particularly useful in palladium-catalyzed cross-coupling reactions to construct complex biaryl structures. Researchers also employ it in material science to synthesize fluorinated liquid crystals or OLED components. Its reactivity enables late-stage functionalization in agrochemical development.

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