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Atomfair 4-Bromo-3,3,4,4-tetrafluoro-1-butene C4H3BrF4

Description 4-Bromo-3,3,4,4-tetrafluoro-1-butene (CAS No. 18599-22-9) is a highly specialized fluorinated organic compound with the molecular formula C4H3BrF4. This halogenated alkene is characterized by its unique structure, featuring a bromine atom and four fluorine atoms attached to a butene backbone, making it a valuable intermediate in advanced synthetic chemistry. With an IUPAC name of 4-bromo-3,3,4,4-tetrafluorobut-1-ene , this compound is available in high purity grades suitable for research and industrial applications. Its reactivity and fluorinated nature make it ideal for use in pharmaceuticals, agrochemicals, and material science. Proper handling under inert conditions is recommended due to its potential sensitivity to moisture and…

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Description

Description

4-Bromo-3,3,4,4-tetrafluoro-1-butene (CAS No. 18599-22-9) is a highly specialized fluorinated organic compound with the molecular formula C4H3BrF4. This halogenated alkene is characterized by its unique structure, featuring a bromine atom and four fluorine atoms attached to a butene backbone, making it a valuable intermediate in advanced synthetic chemistry. With an IUPAC name of 4-bromo-3,3,4,4-tetrafluorobut-1-ene, this compound is available in high purity grades suitable for research and industrial applications. Its reactivity and fluorinated nature make it ideal for use in pharmaceuticals, agrochemicals, and material science. Proper handling under inert conditions is recommended due to its potential sensitivity to moisture and air.

  • CAS No: 18599-22-9
  • Molecular Formula: C4H3BrF4
  • Molecular Weight: 206.96
  • Exact Mass: 205.93543
  • Monoisotopic Mass: 205.93543
  • IUPAC Name: 4-bromo-3,3,4,4-tetrafluorobut-1-ene
  • SMILES: C=CC(C(F)(F)Br)(F)F
  • Synonyms: 4-Bromo-3,3,4,4-tetrafluoro-1-butene, 18599-22-9, 4-Bromo-3,3,4,4-tetrafluorobut-1-ene, 1-Butene, 4-bromo-3,3,4,4-tetrafluoro-, EINECS 242-440-8

Application

4-Bromo-3,3,4,4-tetrafluoro-1-butene is primarily used as a key building block in the synthesis of fluorinated organic compounds. Its applications include serving as an intermediate in the development of pharmaceuticals, agrochemicals, and specialty polymers. The compound’s unique reactivity profile allows for selective functionalization in cross-coupling reactions and nucleophilic substitutions. Researchers also utilize it in the study of fluorinated materials for their unique chemical and physical properties.

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