(2,4,5-Trichlorophenyl) hexanoate

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Identification

Molecular formula
C12H13Cl3O2
CAS Number
16105-63-6
IUPAC Name
(2,4,5-trichlorophenyl) hexanoate
Molecular Weight
295.59g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3738g/cm3
Synonyms
2, 4, 5-trichlorophenyl hexanoate
Interesting facts

Interesting Facts about (2,4,5-Trichlorophenyl) Hexanoate

(2,4,5-Trichlorophenyl) hexanoate, a compound in the realm of organochlorines, offers intriguing insights into its properties and applications. This chemical is a derivative of hexanoic acid, where the phenyl ring is substituted with three chlorine atoms at the 2, 4, and 5 positions. Here are some notable points about this compound:

  • Environmental Impact: Compounds like (2,4,5-trichlorophenyl) hexanoate are often scrutinized for their environmental effects, particularly regarding their persistence and bioaccumulation in ecosystems.
  • Historical Context: The development and use of chlorinated organic compounds, including those similar to this one, have played significant roles in both agricultural and industrial applications.
  • Interference with Biological Systems: Some trichlorophenyl compounds have been examined for their potential to disrupt endocrine functions, raising awareness about their safety and regulatory status.
  • Analytical Techniques: This compound can be effectively studied using modern analytical techniques such as Gas Chromatography-Mass Spectrometry (GC-MS), allowing scientists to understand its distribution and breakdown in various environments.
  • Versatile Applications: While specific applications may vary, compounds like (2,4,5-trichlorophenyl) hexanoate can be utilized in pharmaceuticals, agrochemicals, or as intermediates in synthesis.

In summary, (2,4,5-trichlorophenyl) hexanoate represents the intersection of chemistry, environmental science, and safety, showcasing the need for continued research and awareness surrounding such compounds. As noted by chemists, “The balance between utility and safety is a constant theme in the study of synthetic chemicals.”

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