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1,4-Dichloro-2,3-diiodobut-2-ene

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Identification
Molecular formula
C4H4Cl2I2
CAS number
NA
IUPAC name
1,4-dichloro-2,3-diiodo-but-2-ene
State
State

At room temperature, it is a liquid.

Melting point (Celsius)
12.40
Melting point (Kelvin)
285.55
Boiling point (Celsius)
345.80
Boiling point (Kelvin)
618.95
General information
Molecular weight
361.82g/mol
Molar mass
361.8190g/mol
Density
2.3830g/cm3
Appearence

1,4-Dichloro-2,3-diiodobut-2-ene is a colorless to pale yellow liquid.

Comment on solubility

Solubility of 1,4-Dichloro-2,3-diiodo-but-2-ene

1,4-Dichloro-2,3-diiodo-but-2-ene is a halogenated compound that exhibits interesting solubility properties. When we analyze halogenated organic compounds like this one, several factors come into play:

  • Polarity: The presence of multiple halogen atoms increases the polarity of the molecule, which can affect solubility in various solvents.
  • Hydrophobic vs Hydrophilic: Generally, compounds with significant halogen substitution tend to be less soluble in water, as halogens are hydrophobic in nature. Thus, 1,4-dichloro-2,3-diiodo-but-2-ene may show low solubility in aqueous solutions.
  • Organic Solvents: This compound is likely to be more soluble in organic solvents such as ethanol, chloroform, or dichloromethane due to its non-polar characteristics and the presence of carbon atoms.
  • Temperature Influence: The solubility of the compound may also vary with temperature; typically, increased temperature can enhance solubility, particularly in organic solvents.

In summary, 1,4-dichloro-2,3-diiodo-but-2-ene is expected to show limited solubility in water while having a higher solubility in several organic solvents. This makes it an interesting compound for applications where non-aqueous mixtures are required. As with many halogenated compounds, caution should be exercised regarding their environmental impact and toxicity.

Interesting facts

Interesting Facts About 1,4-Dichloro-2,3-Diiodo-but-2-ene

1,4-Dichloro-2,3-diiodo-but-2-ene is an intriguing organohalogen compound that has garnered attention in various fields of research due to its unique properties. Here are some noteworthy aspects:

  • Biological Activity: This compound exhibits interesting biological properties, which makes it a subject of study in medicinal chemistry. It has been investigated for its potential as a pesticide and as an anticancer agent.
  • Synthesis: The synthesis of 1,4-dichloro-2,3-diiodo-but-2-ene involves multiple halogenation steps, making it a fascinating example of organic synthesis methodologies. Chemists often utilize selective halogenation reactions to achieve the desired compound.
  • Reactivity: Due to the presence of both chlorine and iodine atoms, this compound demonstrates unique reactivity patterns. It is often studied for its ability to participate in nucleophilic substitution reactions and other transformations, offering insight into reaction mechanisms.
  • Applications: Beyond its use in research, 1,4-dichloro-2,3-diiodo-but-2-ene is of interest in materials science, particularly in the development of new polymers or compounds with specific electronic properties.
  • Historical Context: Compounds like this one have played pivotal roles in the advancement of organohalogen chemistry, and understanding their formation has helped chemists develop better methods for synthesizing complex organic molecules.

In summary, 1,4-dichloro-2,3-diiodo-but-2-ene is more than just a chemical formula; it represents a blend of synthetic challenge and potential applications that intrigue both chemists and students alike. Its study not only advances our understanding of organohalogen compounds but also highlights the significance of chemical innovation in science. As stated by renowned chemist Linus Pauling, "Science is the search for truth." This compound exemplifies that search in the realm of organic chemistry.

Synonyms
SCHEMBL9631452