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1,1,2,4-Tetrachlorobut-2-ene

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Identification
Molecular formula
C4H4Cl4
CAS number
760-23-6
IUPAC name
1,1,2,4-tetrachlorobut-2-ene
State
State

1,1,2,4-Tetrachlorobut-2-ene is a liquid at room temperature.

Melting point (Celsius)
-63.00
Melting point (Kelvin)
210.15
Boiling point (Celsius)
115.50
Boiling point (Kelvin)
388.65
General information
Molecular weight
179.90g/mol
Molar mass
179.9020g/mol
Density
1.3800g/cm3
Appearence

1,1,2,4-Tetrachlorobut-2-ene is a colorless to pale yellow liquid. It is typically clear and may have a pungent odor due to its chlorine content.

Comment on solubility

Solubility of 1,1,2,4-tetrachlorobut-2-ene

1,1,2,4-tetrachlorobut-2-ene (C4H4Cl4) exhibits unique solubility characteristics due to its chlorinated structure. Understanding its solubility is crucial for various applications. Here are some key points to consider:

  • Polarity: The presence of multiple chlorine atoms increases the polarity of the molecule, which influences its interaction with solvents.
  • Solvent Compatibility: 1,1,2,4-tetrachlorobut-2-ene is more likely to dissolve in polar organic solvents, such as:
    • Alcohols
    • Aromatics
    • Ethers
  • Water Solubility: It is generally considered to be insoluble in water due to its hydrophobic characteristics stemming from the chlorinated hydrocarbons.
  • Environmental Impact: The solubility in organic solvents can lead to concerns regarding its persistence in the environment, particularly in soil and water.

To summarize, while 1,1,2,4-tetrachlorobut-2-ene can dissolve in various polar organic solvents, it is largely insoluble in water. This behavior is primarily dictated by its molecular structure and the presence of electronegative chlorine atoms, which significantly alter its solubility profile.

Interesting facts

Interesting Facts about 1,1,2,4-Tetrachlorobut-2-ene

1,1,2,4-tetrachlorobut-2-ene is a fascinating compound within the realm of organic chemistry. Its unique structure and chlorinated nature make it noteworthy for several reasons:

  • Industrial Applications: This compound is utilized in the manufacturing of various chemical products, especially in the production of agrochemicals and pesticides.
  • Environmental Persistence: Due to its chlorinated structure, 1,1,2,4-tetrachlorobut-2-ene exhibits greater environmental persistence, leading to concerns about its long-term ecological impact.
  • Reactivity: The presence of multiple chlorine atoms introduces various reaction pathways that are of interest to chemists. Its reactivity can lead to fascinating chemical transformations, such as nucleophilic substitution reactions.
  • Synthetic Routes: Researchers often explore different synthesis pathways to produce this compound, enhancing our understanding of chlorinated compounds and their functionalities.

As chemists continue to investigate 1,1,2,4-tetrachlorobut-2-ene, they uncover more about its chemical properties and applications. It serves as a fine example of how even simple compounds can have complex implications in both industry and environmental science. As one scientist aptly noted: "The beauty of chemistry lies in the potential hidden within each molecule."

Synonyms
DTXSID201031842
1,1,2,4-TETRACHLOROBUT-2-ENE