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1,2,3,4-Tetraiodobenzene

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Identification
Molecular formula
C6H2I4
CAS number
488-22-4
IUPAC name
1,2,3,4-tetraiodobenzene
State
State

At room temperature, 1,2,3,4-tetraiodobenzene is a solid.

Melting point (Celsius)
199.00
Melting point (Kelvin)
472.15
Boiling point (Celsius)
366.00
Boiling point (Kelvin)
639.15
General information
Molecular weight
613.72g/mol
Molar mass
613.7200g/mol
Density
3.5210g/cm3
Appearence

1,2,3,4-Tetraiodobenzene is a crystalline solid that appears white to off-white in color.

Comment on solubility

Solubility of 1,2,3,4-Tetraiodobenzene

1,2,3,4-Tetraiodobenzene, with the chemical formula C6I4H2, is a compound notable for its unique solubility characteristics.

When discussing its solubility, it's important to consider the following factors:

  • Polarity: 1,2,3,4-Tetraiodobenzene is a nonpolar compound due to the presence of four iodine atoms, which make it less soluble in polar solvents.
  • Solvent Compatibility: It tends to dissolve well in nonpolar organic solvents. Examples include:
    • Benzene
    • Toluene
    • Chloroform
  • Water Solubility: 1,2,3,4-Tetraiodobenzene has a very low solubility in water, which can be attributed to its nonpolar character.
  • Temperature Influence: The solubility may vary with temperature, often increasing as temperature rises in nonpolar solvents.

Overall, the solubility profile of 1,2,3,4-tetraiodobenzene can be summarized as follows:

  1. Highly soluble in nonpolar organic solvents
  2. Minimal solubility in polar solvents, particularly in water
  3. Solubility increases with temperature in compatible solvents

In conclusion, understanding the solubility of 1,2,3,4-tetraiodobenzene is crucial for its application in various chemical processes. As the saying goes, "Like dissolves like," and this compound exemplifies that principle effectively.

Interesting facts

Interesting Facts about 1,2,3,4-Tetraiodobenzene

1,2,3,4-Tetraiodobenzene is a remarkable compound that falls under the category of halogenated aromatic hydrocarbons. This compound consists of a benzene ring where four iodine atoms are substituted onto the ring at the 1, 2, 3, and 4 positions. Here are some intriguing insights about this fascinating compound:

  • Unique Structure: The presence of multiple iodine atoms significantly alters the properties of the benzene ring, making it highly reactive and unique among other substituted benzenes.
  • Applications in Synthesis: 1,2,3,4-Tetraiodobenzene serves as a precursor in organic synthesis, particularly in the production of other iodinated compounds. Its ability to donate iodine atoms is invaluable in various reactions.
  • Scientific Research: Researchers have explored its potential applications in materials science and nanotechnology, particularly in the development of novel organic electronic devices.
  • Environmental Considerations: With the increasing focus on environmental sustainability, studies on the degradation and environmental impact of halogenated compounds, including tetraiodobenzene, are essential. This research aids in understanding their persistence and potential toxicity.
  • Behavior in Different States: The compound’s interactions with light and its behavior in different solvents provide insights into its electronic properties, making it an interesting subject for theoretical and experimental chemists alike.

As one delves deeper into the properties and applications of 1,2,3,4-tetraiodobenzene, it's clear that this compound not only enriches the realm of chemistry but also poses challenging questions and applications that scientists are eager to explore. The synthesis and manipulation of such compounds continue to be a hot topic in chemistry, raising new avenues for innovation and discovery.

Synonyms
1,2,3,4-TETRAIODOBENZENE
634-68-4
DTXSID90274511
DTXCID10225984
Tetraiodobenzene
1,2,3,4-Tetrajodbenzol
SCHEMBL797108
BHASHBRUGOYKMC-UHFFFAOYSA-N