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Atomfair Bromodiiodomethane CHBrI2

Description Bromodiiodomethane (CAS No. 57381-39-2) is a highly specialized halogenated methane derivative with the molecular formula CHBrI2. This compound, also known by its IUPAC name bromo(diiodo)methane , is a dense, volatile liquid with applications in organic synthesis and material science. Its unique combination of bromine and iodine atoms makes it a valuable reagent for selective halogenation reactions, cyclopropanation, and as a precursor in the synthesis of complex organoiodine compounds. Packaged under inert gas to ensure stability, our high-purity Bromodiiodomethane (>98%) is ideal for research requiring precise halogen interactions. Available in amber glass vials to prevent photodegradation.

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Description

Description

Bromodiiodomethane (CAS No. 57381-39-2) is a highly specialized halogenated methane derivative with the molecular formula CHBrI2. This compound, also known by its IUPAC name bromo(diiodo)methane, is a dense, volatile liquid with applications in organic synthesis and material science. Its unique combination of bromine and iodine atoms makes it a valuable reagent for selective halogenation reactions, cyclopropanation, and as a precursor in the synthesis of complex organoiodine compounds. Packaged under inert gas to ensure stability, our high-purity Bromodiiodomethane (>98%) is ideal for research requiring precise halogen interactions. Available in amber glass vials to prevent photodegradation.

  • CAS No: 57381-39-2
  • Molecular Formula: CHBrI2
  • Molecular Weight: 346.73
  • Exact Mass: 345.73511
  • Monoisotopic Mass: 345.73511
  • IUPAC Name: bromo(diiodo)methane
  • SMILES: C(Br)(I)I
  • Synonyms: Bromodiiodomethane, 557-95-9, bromo(diiodo)methane, Methane, bromodiiodo-, DTXSID70204235

Application

Bromodiiodomethane is primarily used as a reagent in organic synthesis for the introduction of halogen groups. It serves as a key intermediate in the preparation of iodinated pharmaceuticals and agrochemicals. Researchers utilize its reactivity in cyclopropanation reactions to form strained ring systems. Additionally, it finds niche applications in material science for modifying polymer properties through halogenation.

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