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1,2-Dichlorobuta-1,3-diene

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Identification
Molecular formula
C4H4Cl2
CAS number
1653-19-6
IUPAC name
1,2-dichlorobuta-1,3-diene
State
State

At room temperature, 1,2-dichlorobuta-1,3-diene is a liquid. It is typically handled in liquid form in industrial and research settings.

Melting point (Celsius)
-49.00
Melting point (Kelvin)
224.15
Boiling point (Celsius)
112.40
Boiling point (Kelvin)
385.55
General information
Molecular weight
108.98g/mol
Molar mass
108.9670g/mol
Density
1.1639g/cm3
Appearence

1,2-Dichlorobuta-1,3-diene appears as a colorless liquid. This compound is less commonly encountered in everyday scenarios but is valuable in specialized chemical applications due to its reactivity.

Comment on solubility

Solubility of 1,2-Dichlorobuta-1,3-diene

1,2-Dichlorobuta-1,3-diene, with the chemical formula C4H4Cl2, exhibits distinct solubility characteristics that are influenced by its molecular structure and the presence of chlorine atoms. Here’s an overview of its solubility traits:

  • Polar Solvents: This compound tends to be soluble in polar solvents due to the electronegative chlorine atoms, which create polar covalent bonds.
  • Non-Polar Solvents: Conversely, 1,2-dichlorobuta-1,3-diene may also show some degree of solubility in non-polar solvents, highlighting its amphiphilic nature.
  • Water Solubility: It has limited solubility in water, a characteristic of many organic chlorinated compounds; thus, it is generally considered non-aqueous.
  • Concentration Factors: The actual solubility can vary significantly with concentration, temperature, and the specific solvent used.

In summary, while 1,2-dichlorobuta-1,3-diene demonstrates a preference for solubility in polar environments, the impact of solvent choice and temperature cannot be underestimated. As with many organic compounds, understanding these solubility dynamics is crucial for practical applications.

Interesting facts

Interesting Facts about 1,2-Dichlorobuta-1,3-diene

1,2-Dichlorobuta-1,3-diene is a fascinating compound that belongs to the class of dienes, which are compounds featuring two double bonds. This unique structure allows it to engage in a variety of chemical reactions, making it an important compound in organic chemistry. Here are some intriguing aspects of this compound:

  • Reactive Nature: The presence of both double bonds and chlorine atoms makes this compound highly reactive, especially towards nucleophiles. As such, it can participate in polymerization processes.
  • Synthesis: It can be synthesized through several methods, often involving the chlorination of butadiene. Understanding these synthesis routes is crucial for chemists seeking to create derivatives or utilize the compound in further reactions.
  • Applications: 1,2-Dichlorobuta-1,3-diene serves as a valuable intermediate in the synthesis of various organic compounds, including agrochemicals and pharmaceuticals. Its ability to serve as a building block is crucial in the development of new materials.
  • Environmental Considerations: Like many chlorinated compounds, it is essential to handle 1,2-dichlorobuta-1,3-diene with care. Its persistence in the environment poses potential risks, making studies on degradation and remediation valuable.
  • Structural Insights: Its geometry, which can affect reactivity and properties, is an exciting subject for research. Many chemists conduct computational studies to derive insights about its reactivity and possible pathways in chemical reactions.

In conclusion, 1,2-dichlorobuta-1,3-diene's complex structure and reactive characteristics underscore its significance in both academic research and industrial applications. As noted by many chemists, "Understanding the subtle nuances of such compounds opens doors to innovative solutions in material science."
Its study continues to be a source of intrigue and opportunity in the field of organic chemistry.

Synonyms
SCHEMBL7106364
SCHEMBL9842776
1,2-dichloro-buta-1,3-diene
SCHEMBL28323654