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2,3,5,6-Tetrachloroterephthaloyl chloride

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Identification
Molecular formula
C8HCl6O2
CAS number
937-89-5
IUPAC name
2,3,5,6-tetrachlorobenzene-1,4-dicarbonyl chloride
State
State

At room temperature, 2,3,5,6-Tetrachlorobenzene-1,4-dicarbonyl chloride is in a solid state. Its specific structure, with multiple chlorine atoms, results in a more stable solid form suitable for various industrial applications.

Melting point (Celsius)
109.00
Melting point (Kelvin)
382.15
Boiling point (Celsius)
257.00
Boiling point (Kelvin)
530.15
General information
Molecular weight
295.90g/mol
Molar mass
295.9000g/mol
Density
1.8000g/cm3
Appearence

2,3,5,6-Tetrachlorobenzene-1,4-dicarbonyl chloride typically appears as a white to light yellow crystalline solid. It may display a slightly aromatic odor due to its chlorinated benzene rings. This compound is not very soluble in water but is soluble in organic solvents like toluene and chloroform. The presence of multiple chlorine atoms in the structure can impart it with a distinct coloration and odor characteristic of organochlorides.

Comment on solubility

Solubility of 2,3,5,6-Tetrachlorobenzene-1,4-Dicarbonyl Chloride

The solubility of 2,3,5,6-tetrachlorobenzene-1,4-dicarbonyl chloride is an intriguing aspect that merits discussion. This compound, characterized by its multiple chlorinated benzene rings and dicarbonyl functionality, demonstrates unique solubility behaviors due to its structural properties.

Key solubility characteristics include:

  • Solvent Compatibility: It is expected to exhibit better solubility in polar organic solvents such as dimethyl sulfoxide (DMSO) or chloroform, while being less soluble in non-polar solvents.
  • Temperature Dependency: Like many organic compounds, its solubility may increase with temperature, allowing for greater dissolution in solvent matrices.
  • Chlorinated Nature: The presence of multiple chlorine atoms generally enhances hydrophobic interactions, potentially leading to limited solubility in aqueous environments.

In summary, while the solubility behavior of 2,3,5,6-tetrachlorobenzene-1,4-dicarbonyl chloride may not be extensively detailed in literature, it is clear that factors such as solvent type, temperature, and molecular characteristics play crucial roles in determining its solubility profile. Understanding these aspects is essential for applications ranging from synthesis to environmental impact assessments.

Interesting facts

Interesting Facts About 2,3,5,6-Tetrachlorobenzene-1,4-dicarbonyl Chloride

2,3,5,6-tetrachlorobenzene-1,4-dicarbonyl chloride is a fascinating compound that plays an essential role in various chemical processes and applications. This compound offers intriguing characteristics and utility, making it a topic of interest for both chemists and environmental scientists.

Key Features:

  • Halogenated Compound: This compound contains multiple chlorine atoms, which significantly enhance its reactivity and stability compared to non-halogenated compounds.
  • Versatile Intermediate: It serves as an important intermediate in the synthesis of various organic compounds, especially in the production of herbicides and fungicides.
  • Environmental Considerations: Due to its chlorinated nature, it is crucial to study the environmental impact of such compounds, particularly regarding their persistence and potential bioaccumulation.

The presence of both carbonyl and dichloride functional groups contributes to its unique reactivity profile. As a scientist, one might say, *"Understanding the reactivity of halogenated compounds like this one can unlock new pathways for synthetic chemistry."* This quote emphasizes the compound's importance in developing new synthetic methods and products.

Applications:

  • Agricultural Chemicals: Used in the formulation of pesticides and herbicides, aiding in crop protection.
  • Pharmaceuticals: Potential precursor in the synthesis of biologically active molecules.
  • Material Science: Explored for incorporation in polymer chemistry to produce chlorinated polymers.

Overall, 2,3,5,6-tetrachlorobenzene-1,4-dicarbonyl chloride is not only significant for its chemical properties but also for its implications in environmental science and industrial applications. Further research into this compound can yield advancements across various fields!

Synonyms
2,3,5,6-Tetrachloroterephthaloyl dichloride
719-32-4
Tetrachloroterephthaloyl chloride
Tetrachloroterephthaloyl dichloride
2,3,5,6-TETRACHLOROTEREPHTHALOYL CHLORIDE
Tetrachloroterephthalic dichloride
Terephthaloyl chloride, tetrachloro-
Perchloroterephthaloyl chloride
1,4-Benzenedicarbonyl dichloride, 2,3,5,6-tetrachloro-
CM96O90UX1
HSDB 5749
EINECS 211-947-6
NSC-141495
NSC 141495
2,3,5,6-TETRACHLOROTEREPHTHALIC DICHLORIDE
2,3,5,6-TETRACHLOROTEREPHTHALOYL CHLORIDE [HSDB]
Terephthaloyl chloride, tetrachloro
1,4Benzenedicarbonyl dichloride, 2,3,5,6tetrachloro
211-947-6
2,3,5,6-tetrachlorobenzene-1,4-dicarbonyl chloride
DTXSID5027302
2,3,5,6-Tetrachlorobenzene-1,4-dicarbonyl dichloride
DTXCID107302
CAS-719-32-4
UNII-CM96O90UX1
MFCD00018801
SCHEMBL103420
CHEMBL3186921
Tox21_201449
Tox21_303098
NSC141495
tetrachloroterephthalic acid dichloride
AKOS015891213
2,5,6-Tetrachloroterephthaloyl chloride
NCGC00249049-01
NCGC00257103-01
NCGC00259000-01
2,5,6-Tetrachloroterephthaloyl dichloride
DB-019670
2,3,5,6-Tetrachloro-terephthaloyl chloride
NS00003217
2,3,5,6-TETRACHLOROTEREPHTHALOYLDICHLORIDE
A837362
Q27275531
2,3,5,6-tetrakis(chloranyl)benzene-1,4-dicarbonyl chloride