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Tetraiodothiophene

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Identification
Molecular formula
C4HI4S
CAS number
13118-64-6
IUPAC name
2,3,4,5-tetraiodothiophene
State
State

At room temperature, tetraiodothiophene is typically in a solid state. The compound forms a crystalline structure due to its molecular arrangement.

Melting point (Celsius)
182.00
Melting point (Kelvin)
455.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
581.69g/mol
Molar mass
581.6920g/mol
Density
3.9770g/cm3
Appearence

Tetraiodothiophene appears as a solid compound, typically forming crystalline structures. The crystals are usually dark in color, due to the high iodine content in the compound.

Comment on solubility

Solubility of 2,3,4,5-tetraiodothiophene

2,3,4,5-tetraiodothiophene, a compound with intriguing chemical properties, exhibits specific solubility characteristics that are important to consider. Understanding its solubility helps in various applications and reactions involving this compound.

General Solubility Insights

This compound is generally known to be:

  • Insoluble in water: The presence of iodine atoms enhances hydrophobic interactions, making it poorly soluble in polar solvents like water.
  • Soluble in organic solvents: It tends to dissolve well in non-polar to moderately polar organic solvents (e.g., chloroform, benzene, or dichloromethane), which is common for larger molecular compounds.

Factors Influencing Solubility

Several factors can influence the solubility of 2,3,4,5-tetraiodothiophene:

  1. Molecular Structure: The bulky iodine substituents contribute to its unique solubility profiles.
  2. Temperature: Higher temperatures usually increase solubility in organic solvents.
  3. Interaction with Solvent: The compatibility of solute and solvent polarities significantly affects solubility.

In summary, while 2,3,4,5-tetraiodothiophene shows limited solubility in water, its solubility in various organic solvents highlights its versatility in chemical reactions and applications. This unique behavior emphasizes the necessity of understanding solubility in the context of chemical research and formulation development.

Interesting facts

Interesting Facts about 2,3,4,5-Tetraiodothiophene

2,3,4,5-Tetraiodothiophene is a fascinating compound that belongs to the family of organosulfur compounds. Its unique structure and properties make it an interesting subject of study in both organic chemistry and materials science. Here are some compelling facts about this compound:

  • Halogenation Power: The presence of four iodine atoms in the structure gives this compound remarkable halogenation capabilities, making it a candidate for various chemical reactions.
  • Electronic Properties: The substitution of iodine significantly influences its electronic properties, possibly enhancing its conductivity—an interesting aspect for applications in electronic devices.
  • Environmental Applications: Research is ongoing into the potential uses of tetraiodothiophenes in photodynamic therapy and environmental remediation, owing to their ability to absorb light and potentially break down hazardous substances.
  • Structural Versatility: The thiophene ring offers a degree of structural versatility, allowing chemists to modify its properties further. Different substituents can provide a wide range of functional properties useful in various applications.

The exploration of 2,3,4,5-tetraiodothiophene isn't just limited to theoretical studies; practical applications in materials science and organic electronics represent a promising avenue for future research.
Given its intriguing characteristics, this compound could contribute significantly to advancements in chemistry and technology, proving that the world of chemical compounds is vast and full of potential!

Synonyms
Tetraiodothiophene
19259-11-1
THIOPHENE, TETRAIODO-
2,3,4,5-Tetraiodothiophene
Thiophene, 2,3,4,5-tetraiodo-
C4I4S
EINECS 242-924-9
NSC 109401
BRN 0118445
NSC99446
4-17-00-00255 (Beilstein Handbook Reference)
SCHEMBL11297497
DTXSID00172857
VWDOXSASHQWCRB-UHFFFAOYSA-N
MFCD00014524
NSC-99446
NSC109401
AKOS015964913
NSC-109401
DB-299284
NS00026283