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Atomfair 5-Bromo-2-iodotoluene C7H6BrI

Description 5-Bromo-2-iodotoluene (CAS No. 202865-85-8) is a high-purity halogenated aromatic compound with the molecular formula C7H6BrI and IUPAC name 4-bromo-1-iodo-2-methylbenzene . This versatile intermediate is rigorously synthesized and purified to meet the stringent demands of pharmaceutical, agrochemical, and materials science research. Its unique structure, featuring both bromine and iodine substituents on a toluene backbone, makes it an exceptionally valuable building block for cross-coupling reactions (e.g., Suzuki, Stille, Negishi) and functional group transformations. Provided in sealed amber vials under inert atmosphere to ensure stability, our product undergoes comprehensive QC including GC/MS, NMR, and elemental analysis. Available in research (1g, 5g) and…

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Description

Description

5-Bromo-2-iodotoluene (CAS No. 202865-85-8) is a high-purity halogenated aromatic compound with the molecular formula C7H6BrI and IUPAC name 4-bromo-1-iodo-2-methylbenzene. This versatile intermediate is rigorously synthesized and purified to meet the stringent demands of pharmaceutical, agrochemical, and materials science research. Its unique structure, featuring both bromine and iodine substituents on a toluene backbone, makes it an exceptionally valuable building block for cross-coupling reactions (e.g., Suzuki, Stille, Negishi) and functional group transformations. Provided in sealed amber vials under inert atmosphere to ensure stability, our product undergoes comprehensive QC including GC/MS, NMR, and elemental analysis. Available in research (1g, 5g) and bulk (25g, 100g) quantities with customizable packaging options.

  • CAS No: 202865-85-8
  • Molecular Formula: C7H6BrI
  • Molecular Weight: 296.93
  • Exact Mass: 295.86976
  • Monoisotopic Mass: 295.86976
  • IUPAC Name: 4-bromo-1-iodo-2-methylbenzene
  • SMILES: CC1=C(C=CC(=C1)Br)I
  • Synonyms: 5-Bromo-2-iodotoluene, 116632-39-4, DTXSID60369180, DTXCID60320216, 629-570-4

Application

5-Bromo-2-iodotoluene serves as a critical precursor in palladium-catalyzed cross-coupling reactions for synthesizing biaryl compounds in drug discovery. The compound’s differential halogen reactivity enables sequential functionalization, making it valuable for creating molecular scaffolds in material science. Researchers utilize it to develop liquid crystals and OLED materials due to its stable aromatic core with heavy atom effects.

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