1,2,3-trichloro-1,1,2,3,4,4,4-heptafluoro-butane

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Identification

Molecular formula
C4HCl3F7
CAS Number
42594-17-2
IUPAC Name
1,2,3-trichloro-1,1,2,3,4,4,4-heptafluoro-butane
Molecular Weight
277.37g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
and relatively low boiling points compared to hydrocarbons of similar molar mass.
Synonyms
1, 2, 3-trichloro-1, 1, 2, 3, 4, 4, 4-heptafluorobutane
Interesting facts

Interesting Facts about 1,2,3-Trichloro-1,1,2,3,4,4,4-Heptafluoro-Butane

1,2,3-Trichloro-1,1,2,3,4,4,4-heptafluoro-butane is a fascinating compound known for its unique chemical structure and diverse applications. Here are some intriguing facts:

  • Highly Fluorinated: This compound features a remarkable number of fluorine atoms, making it one of the more heavily fluorinated organic compounds. Its extensive fluorination contributes to its stability and resistance to degradation.
  • Relevance in Industrial Applications: Due to its properties, this trichloroheptafluorobutane is utilized in various industrial applications, particularly in the production of refrigerants and solvents.
  • Environmental Considerations: Like many halogenated compounds, it raises environmental concerns due to its potential to contribute to ozone layer depletion. Understanding its impact is crucial for compliance with international regulations.
  • Structure-Activity Relationship: The combination of chlorinated and fluorinated substituents provides insights into structure-activity relationships (SAR), which are significant in medicinal chemistry and the development of new materials.
  • Chirality: The compound can exhibit chirality due to its asymmetric carbon centers. Chirality is a vital concept in chemistry that often influences the biological activity of compounds.

In summary, 1,2,3-trichloro-1,1,2,3,4,4,4-heptafluoro-butane is not only a compound of industrial relevance but also a study subject for environmental scientists and chemists alike. The interaction of its various functional groups allows for a wide range of chemical behavior and applications.

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