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.
Synonyms
1,2,3-trichloro-1,1,2,3,4,4,4-heptafluorobutane
SCHEMBL1899391
ICVLETFDTDJCDT-UHFFFAOYSA-N
Solubility of 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, often referred to by its commercial name, is a compound notable for its unique solubility characteristics.
This compound is generally considered to be:
As is often the case with halogenated compounds, the solubility profile can be attributed to the balance between polar and non-polar interactions within the molecule. The strong electronegativity of fluorine, combined with the presence of chlorine, results in a molecule that's quite different in solubility compared to simpler hydrocarbons. This also highlights a critical concept in chemistry: "Like dissolves like." In other words, the best solvents for 1,2,3-trichloro-1,1,2,3,4,4,4-heptafluoro-butane are non-polar and weakly polar solvents that can interact adequately with its unique structure.