Skip to main content

2,8-Dichlorodibenzofuran

ADVERTISEMENT
Identification
Molecular formula
C12H6Cl2O
CAS number
135-50-4
IUPAC name
2,8-dichlorodibenzofuran
State
State

At room temperature, 2,8-Dichlorodibenzofuran is primarily in a solid state. It is stable under ordinary conditions of use and storage, but care should be taken to avoid exposure to heat sources, as it can emit toxic fumes when decomposed.

Melting point (Celsius)
146.00
Melting point (Kelvin)
419.15
Boiling point (Celsius)
345.00
Boiling point (Kelvin)
618.15
General information
Molecular weight
251.09g/mol
Molar mass
251.0900g/mol
Density
1.4190g/cm3
Appearence

2,8-Dichlorodibenzofuran typically appears as a white crystalline solid. Its solid state can vary slightly in color under different environmental conditions due to lighting, impurities, or particle size.

Comment on solubility

Solubility of 2,8-Dichlorodibenzofuran

2,8-Dichlorodibenzofuran is a compound of particular interest when discussing its solubility characteristics, which are influenced by several factors:

  • Polarity: The presence of chlorine substituents on the dibenzofuran structure can affect the overall polarity of the compound. Chlorine atoms are electronegative, thus making the compound moderately polar, which may enhance its solubility in polar solvents.
  • Solvent Compatibility: Typically, 2,8-dichlorodibenzofuran is expected to have better solubility in organic solvents due to its hydrophobic nature. Solvents such as acetone, dichloromethane, and ethyl acetate are likely effective.
  • Temperature Influence: Like many organic compounds, the solubility of 2,8-dichlorodibenzofuran generally increases with temperature. This principle can be a helpful consideration during experimentation.

Additionally, studies have indicated that the solubility in water is quite limited, adhering to the typical behavior of halogenated organic compounds. As a result:

  • It is relatively insoluble in water.
  • It shows increased solubility in organic solvents.

In summary, understanding the solubility of 2,8-dichlorodibenzofuran not only enriches our knowledge of its chemical behavior but is also essential for its application in various chemical processes and environmental assessments.

Interesting facts

Interesting Facts About 2,8-Dichlorodibenzofuran

2,8-Dichlorodibenzofuran is a fascinating chemical compound that piques the interest of scientists and researchers alike. Here are some intriguing insights into this compound:

  • Structural Composition: This compound features a dibenzofuran skeleton, which consists of a fused structure of two benzene rings connected by a furan ring. The unique nature of this structure allows for various derivatives, making dibenzofurans an important class in organic chemistry.
  • Chlorination Significance: The presence of two chlorine atoms at the 2 and 8 positions significantly affects the compound's reactivity and properties. Chlorination often enhances stability, which can be crucial in different chemical processes.
  • Toxicological Profile: Like many chlorinated compounds, 2,8-dichlorodibenzofuran has been studied for its toxicological implications. Research indicates that chlorinated dibenzofurans can have environmental persistence and potential bioaccumulation, raising concerns about their ecological impact.
  • Applications in Science: This compound may not have a broad industrial application, but it serves as a valuable tool in chemical synthesis and research. It helps scientists understand reaction mechanisms and the behavior of chlorinated aromatic compounds.
  • Research and Regulation: Owing to its chlorinated structure, 2,8-dichlorodibenzofuran falls under scrutiny by environmental agencies. Understanding its degradation and bioactivity is crucial for evaluating the safety and regulations surrounding similar compounds.

In summary, 2,8-dichlorodibenzofuran stands as a significant compound in organic chemistry, with its unique structure and properties offering valuable insights into both synthetic applications and environmental considerations. As research continues, this compound could lead to discoveries that illuminate the complex interactions of organic compounds in our environment.

Synonyms
2,8-DICHLORODIBENZOFURAN
5409-83-6
2,8-Dichlorodibenzo[b,d]furan
Dibenzofuran, 2,8-dichloro-
UNII-GNF0836UQJ
GNF0836UQJ
NSC 12535
NSC-12535
PCDF 16
DTXSID30871129
DICHLORODIBENZOFURAN, 2,8-
2,8-Dichlorodibenzo(b,D)furan
4,12-dichloro-8-oxatricyclo(7.4.0.02,7)trideca-1(13),2,4,6,9,11-hexaene
4,12-dichloro-8-oxatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene
8-Dichloro-dibenzofuran
Dibenzofuran, 2,8dichloro
DTXCID20818801
Dibenzofuran, 2,8-dichloro-(8CI)
Dibenzofuran, 2,8-dichloro-(8CI)(9CI)
637-261-0
ivvrjidvyspkfz-uhfffaoysa-n
2,8-Dichloro-dibenzofuran
CHEMBL140187
NSC12535
Dibenzofuran,8-dichloro-
SCHEMBL2282515
BDBM50408297
AKOS024338441
NS00122391
Q27279195
Dibenzofuran, 2,8-dichloro-; 2,8-Dichlorodibenzofuran; NSC 12535; PCDF 16; 2,8-DCDF