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2,2,2-Tribromoethyl acetate

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Identification
Molecular formula
C4H5Br3O2
CAS number
594-57-4
IUPAC name
2,2,2-tribromoethyl acetate
State
State

At room temperature, 2,2,2-Tribromoethyl acetate is in a liquid state.

Melting point (Celsius)
-40.00
Melting point (Kelvin)
233.15
Boiling point (Celsius)
208.00
Boiling point (Kelvin)
481.15
General information
Molecular weight
344.78g/mol
Molar mass
344.7760g/mol
Density
2.1570g/cm3
Appearence

2,2,2-Tribromoethyl acetate is typically a colorless or light yellow liquid. Its appearance can vary slightly with source and purity.

Comment on solubility

Solubility of 2,2,2-Tribromoethyl Acetate

2,2,2-Tribromoethyl acetate, with the chemical formula C5H6Br3O2, displays intriguing solubility characteristics that make it noteworthy in chemical studies.

When we discuss its solubility, here are some key points to consider:

  • Polar Solvent Compatibility: This compound is likely to be soluble in polar organic solvents due to the presence of the acetate group, which can interact favorably with polar environments.
  • Water Solubility: Given its halogen content and organic nature, 2,2,2-tribromoethyl acetate is expected to have low solubility in water. The bulky bromine atoms can hinder its ability to form hydrogen bonds with water molecules.
  • Other Solvents: It may dissolve better in non-polar solvents, although the extent of this solubility can vary widely depending on the solvent's specific properties.

In summary, the solubility of 2,2,2-tribromoethyl acetate is predominantly influenced by its structure. As encapsulated in the phrase:

"Solubility is a reflection of chemical compatibility."

Understanding these solubility traits is essential for effective application in chemical reactions and product formulations.

Interesting facts

Interesting Facts About 2,2,2-Tribromoethyl Acetate

2,2,2-Tribromoethyl acetate is a fascinating compound with a variety of intriguing applications and properties. This compound, a halogenated ester, is known for its unique chemical structure and reactivity, leading to several noteworthy characteristics.

Key Characteristics

  • Halogenation: The presence of three bromine atoms is significant because halogenated compounds often exhibit enhanced biological activity and reactivity compared to their non-halogenated counterparts.
  • Use in Organic Synthesis: 2,2,2-Tribromoethyl acetate is frequently employed in organic reactions, particularly in the formation of various functional groups and as an electrophile in nucleophilic substitution reactions.
  • Biological Activity: Some studies suggest that halogenated compounds can possess antimicrobial properties, making this compound of interest in pharmaceutical research.
  • Solvent Properties: It is utilized as a solvent in various chemical processes owing to its ability to dissolve a wide range of organic compounds.

Applications in Research and Industry

This compound is not only significant in academic research but also has implications in industrial applications:

  • In the field of pesticide synthesis, it aids in the development of effective agents due to its reactive nature.
  • In material science, it serves as a building block for the synthesis of complex molecules used in various polymers.
  • Its unique properties have drawn interest in the study of drug development, particularly in identifying new therapeutic agents.

A Final Thought

As with many halogenated compounds, safety and environmental considerations must be taken into account when handling 2,2,2-tribromoethyl acetate. The effects of brominated compounds on health and ecosystems are subjects of ongoing research, reinforcing the need for responsible usage in both laboratory and industrial settings. In the words of chemists, "While these compounds can lead to incredible innovations, they also require careful stewardship."


Synonyms
Tribromoethyl acetate
2,2,2-tribromoethyl acetate
Acetic acid, ester with tribromoethanol
BRN 1762051
SCHEMBL9579361
DTXSID10975311
3-02-00-00485 (Beilstein Handbook Reference)