Skip to main content

2,3-Dichlorobutadiene

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

At room temperature, 2,3-dichlorobutadiene is in a liquid state.

Melting point (Celsius)
-47.00
Melting point (Kelvin)
226.15
Boiling point (Celsius)
94.00
Boiling point (Kelvin)
367.15
General information
Molecular weight
108.96g/mol
Molar mass
108.9550g/mol
Density
1.1920g/cm3
Appearence

2,3-Dichlorobutadiene is a colorless liquid with a characteristic odor. It can be described as having a transparent appearance in its pure form.

Comment on solubility

Solubility of 2,3-Dichlorobuta-1,3-diene (C4H4Cl2)

2,3-Dichlorobuta-1,3-diene is a fascinating compound with unique solubility characteristics. Understanding its solubility can be crucial for various applications in chemistry.

Key Points:

  • Solvent Compatibility: This compound is primarily soluble in organic solvents due to its relatively non-polar nature. Common organic solvents such as hexane or ethyl acetate are good choices for dissolving this compound.
  • Water Solubility: 2,3-Dichlorobuta-1,3-diene is not soluble in water. This is primarily due to its low polarity and the presence of chlorine atoms, which can influence its interaction with water molecules.
  • Temperature Dependency: The solubility of 2,3-dichlorobuta-1,3-diene can vary with temperature. Generally, an increase in temperature can enhance the solubility in organic solvents.

In summary, while 2,3-dichlorobuta-1,3-diene exhibits significant solubility in organic solvents, its insolubility in water highlights its non-polar characteristics. As with many chemical compounds, understanding the solubility behavior is essential for effective handling and application in chemical processes.

Interesting facts

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

2,3-Dichlorobuta-1,3-diene is a fascinating compound in the world of organic chemistry, primarily due to its unique structural features and reactivity. Here are some key highlights:

  • Reactivity: This compound is an example of a conjugated diene, which means it contains alternating double bonds. This configuration makes it particularly reactive and interesting for synthetic applications.
  • Natural Occurrence: Compounds similar to 2,3-dichlorobuta-1,3-diene can be found in various natural products and metabolites. Studying these compounds helps scientists understand the mechanisms of natural synthesis.
  • Applications in Synthesis: Due to its structure, 2,3-dichlorobuta-1,3-diene can undergo various reactions, including Diels-Alder reactions, making it useful in the synthesis of more complex molecules.
  • Environmental Aspects: Halogenated compounds such as this one often raise questions concerning their environmental impact, particularly regarding their degradation products and potential toxicity.
  • Historical Relevance: Studying compounds like this has historical significance in the development of modern organic chemistry. Researchers in the mid-20th century focused on halogenated compounds for their unique properties.

As a compound with both industrial and academic relevance, 2,3-dichlorobuta-1,3-diene exemplifies the intricate interplay between structure and reactivity in organic molecules. Its study encourages further exploration and innovation in chemical synthesis.

Synonyms
2,3-Dichloro-1,3-butadiene
2,3-Dichlorobutadiene
1653-19-6
1,3-Butadiene, 2,3-dichloro-
SG9RMT8EAJ
BRN 1698807
EINECS 216-721-0
DTXSID1027423
EC 216-721-0
DTXCID307423
216-721-0
4-01-00-00986 (beilstein handbook reference)
2,3-DICHLOROBUTA-1,3-DIENE
2,3-Dichlor-1,3-butadien
2,3-Dichlorobutadiene-1,3
2,3-Dichlor-1,3-butadien [Czech]
UNII-SG9RMT8EAJ
SCHEMBL125620
NS00006262
Q26840785