Skip to main content

1,4-dichlorobuta-1,3-diene

ADVERTISEMENT
Identification
Molecular formula
C4H4Cl2
CAS number
2404-55-1
IUPAC name
(1E,3E)-1,4-dichlorobuta-1,3-diene
State
State
Liquid at room temperature. It is usually handled in its liquid form due to its low melting point.
Melting point (Celsius)
-58.00
Melting point (Kelvin)
215.15
Boiling point (Celsius)
145.00
Boiling point (Kelvin)
418.15
General information
Molecular weight
127.01g/mol
Molar mass
127.0080g/mol
Density
1.1800g/cm3
Appearence

1,4-dichlorobuta-1,3-diene is a colorless liquid under standard conditions.

Comment on solubility

Solubility of (1E,3E)-1,4-dichlorobuta-1,3-diene

(1E,3E)-1,4-dichlorobuta-1,3-diene, with its unique structure, offers insights into its solubility characteristics. Here are some key points to consider:

  • Polarity: The presence of chlorine atoms introduces polar characteristics, which typically enhance solubility in polar solvents, such as alcohols and ethers.
  • Hydrophobicity: The diene structure contributes a degree of hydrophobicity, potentially limiting its solubility in water.
  • Common Solvents: This compound is likely to dissolve well in organic solvents, including:
    • Acetone
    • Ethanol
    • Chloroform
  • Water Solubility: It is expected to have low water solubility due to its molecular structure.

In summary, while (1E,3E)-1,4-dichlorobuta-1,3-diene may exhibit favorable solubility in certain organic solvents, its overall solubility profile highlights a complex balance between polar and non-polar interactions, making it primarily suitable for non-aqueous environments.

Interesting facts

Interesting Facts about (1E,3E)-1,4-Dichlorobuta-1,3-diene

(1E,3E)-1,4-Dichlorobuta-1,3-diene is a fascinating compound known for its unique structure and wide array of applications in chemistry. Below are some engaging insights into this intriguing chemical:

  • Structure and Isomerism: This compound is an example of a diene, containing two double bonds, which allows for interesting isomeric forms. The 1E and 3E notations indicate the configuration of these double bonds, significantly influencing the compound's reactivity and physical properties.
  • Synthesis: This dichloride can be synthesized through various organic reactions, such as dehydrochlorination reactions, showcasing the fascinating methodologies chemists apply to construct complex molecules.
  • Reactivity: Due to the presence of double bonds, (1E,3E)-1,4-dichlorobuta-1,3-diene is highly reactive. It can participate in Diels-Alder reactions, making it an excellent candidate for creating more complex molecular architectures in organic synthesis.
  • Applications: This compound finds its uses not only in laboratory settings but also in the pharmaceutical and agrochemical industries. It can serve as an intermediate in the synthesis of various valuable compounds.
  • Environmental Impact: Understanding the reactivity and degradation pathways of this compound is essential, as certain dichlorinated organic compounds can present environmental concerns. Studying these compounds contributes to sustainability and the development of greener chemistry processes.
  • Research Significance: The study of (1E,3E)-1,4-dichlorobuta-1,3-diene and related compounds has increased in prominence as researchers seek avenues for optimizing molecular efficiency and exploring novel applications.

In summary, (1E,3E)-1,4-dichlorobuta-1,3-diene is not just another chemical compound; it stands as a testament to the complexity and beauty of organic chemistry, paving the way for innovation and exploration in various scientific fields.

Synonyms
1,4-DICHLORO-1,3-BUTADIENE
2984-42-1
RefChem:1053258
1,3-Butadiene, 1,4-dichloro-
SCHEMBL9335777
LDZSRRMBFGBOAE-ZPUQHVIOSA-N
(E,E)-1,4-Dichloro-1,3-butadiene
(1E,3E)-1,4-Dichloro-1,3-butadiene #