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Bis(4-chlorophenyl) disulfide

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Identification
Molecular formula
C12H8Cl2S2
CAS number
1192-52-5
IUPAC name
1-chloro-4-[(4-chlorophenyl)disulfanyl]benzene
State
State

At room temperature, bis(4-chlorophenyl) disulfide is in a solid state. It forms a crystalline powder that is stable under standard conditions.

Melting point (Celsius)
58.00
Melting point (Kelvin)
331.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
285.22g/mol
Molar mass
285.1950g/mol
Density
1.4767g/cm3
Appearence

Bis(4-chlorophenyl) disulfide typically appears as a white to off-white crystalline powder. It may also sometimes be observed in a slightly beige hue depending on purity levels.

Comment on solubility

Solubility of 1-chloro-4-[(4-chlorophenyl)disulfanyl]benzene

The solubility of 1-chloro-4-[(4-chlorophenyl)disulfanyl]benzene in various solvents is quite specific and can be influenced by factors such as polarity and temperature. In general, such organochlorine compounds tend to exhibit lower solubility in polar solvents due to their hydrophobic nature.

Key Points about Solubility:

  • Polarity: With its chlorine atoms and disulfide linkage, the compound is less likely to dissolve in water.
  • Solvent Compatibility: It may have better solubility in non-polar organic solvents like benzene or toluene.
  • Temperature Effects: Higher temperatures can enhance solubility in various solvents.

In practical terms, it is essential to note that the presence of the disulfide group can impart certain characteristics, influencing solubilization processes. In the context of chemical reactions, solubility can play a critical role in determining reaction kinetics and mechanisms. As a chemical scientist, understanding these nuances helps in predicting behaviors during experimental procedures and applications.

In summary, while 1-chloro-4-[(4-chlorophenyl)disulfanyl]benzene may challenge solubility in polar media, targeting appropriate organic solvents enhances its accessibility for various uses in research and industry.

Interesting facts

1-Chloro-4-[(4-chlorophenyl)disulfanyl]benzene

1-Chloro-4-[(4-chlorophenyl)disulfanyl]benzene, often referred to in shorthand as a disulfide compound, showcases intriguing aspects related to both its chemical structure and applications in various fields. Here are some fascinating facts:

  • Disulfide Bonds: This compound contains disulfide linkages, which are crucial in biochemistry for stabilizing protein structures. Such bonds can significantly influence the 3D arrangement of proteins.
  • Chlorinated Aromatics: The presence of chlorinated groups in its structure is indicative of a class of compounds known for their various applications, including use as pesticides, solvents, and in synthesis.
  • Research Applications: 1-Chloro-4-[(4-chlorophenyl)disulfanyl]benzene may be utilized in organic synthesis, aiding in the formation of complex molecules that are valuable in pharmaceuticals and materials science.
  • Environmental Impact: Understanding compounds like this is essential for assessing environmental impact, as chlorinated compounds can persist in the environment and may have toxicological implications.
  • Potential in Medicinal Chemistry: Compounds containing disulfide linkages are of interest in medicinal chemistry due to their unique properties, such as their ability to modulate biological activity.

As noted in scientific literature, "The exploration of disulfide-containing compounds allows for a greater understanding of their role in biological systems and as therapeutic agents." This encapsulates the dual nature of 1-chloro-4-[(4-chlorophenyl)disulfanyl]benzene, standing at the crossroads of chemistry, biology, and environmental science.

In summary, the study of this compound not only deepens our understanding of chemical interactions but also opens avenues for new discoveries in various scientific domains.

Synonyms
1142-19-4
Bis(4-chlorophenyl) disulfide
4,4'-Dichlorodiphenyl disulfide
Disulfide, bis(4-chlorophenyl)
Di(p-chlorophenyl) disulfide
DDDS (pesticide)
Disulfide, bis(p-chlorophenyl)
p-Chlorophenyl disulfide
4-Chlorophenyl disulfide
Bis(p-chlorophenyl) disulfide
p,p'-Dichlorodiphenyl disulfide
Bis(4-chlorophenyl) disulphide
BIS(P-CHLOROPHENYL)DISULFIDE
NSC 32025
NSC-32025
NSC 677444
HSDB 2791
EINECS 214-531-2
NMT539C7LN
AI3-16362
NSC-677444
Disulfide, bis[4-chlorophenyl]
DTXSID7061562
BIS-(4-CHLOROBENZENE)-DISULFIDE
DDDS [PESTICIDE]
4,4'-DICHLORODIPHENYL DISULFIDE [HSDB]
pChlorophenyl disulfide
Di(pchlorophenyl) disulfide
Bis(4chlorophenyl) disulfide
Disulfide, bis(pchlorophenyl)
Disulfide, bis(4chlorophenyl)
p,p'Dichlorodiphenyl disulfide
4,4'Dichlorodiphenyl disulfide
DTXCID4033344
DDDS
1-Chloro-4-[(4-chlorophenyl)disulfanyl]benzene
1,2-bis(4-chlorophenyl)disulfane
BIS(4-CHLOROPHENYL)DISULFIDE
CHEMBL121019
NSC32025
NSC677444
1,1'-disulfanediylbis(4-chlorobenzene)
C12H8Cl2S2
UNII-NMT539C7LN
Bis(4-chlorophenyl)disulphide
MFCD00013642
di(4-chlorophenyl)disulfide
bis(p-chlorophenyl)disulphide
bis(p-chlorophenyl)-disulfide
di(4-chlorophenyl) disulfide
SCHEMBL162332
4,4'-Dichlorophenyl disulfide
bis-(4-chloro-phenyl)disulfide
ZIXXRXGPBFMPFD-UHFFFAOYSA-
BDBM50555857
NSC823871
STK820839
Bis(4-chlorophenyl) disulfide, 97%
AKOS001092350
CS-W013999
NSC-823871
4,4\'-DICHLORODIPHENYL DISULFIDE
AC-16467
AS-60151
PD168657
DB-041205
D0360
NS00023707
1-chloro-4-(4-chlorophenyl)disulfanylbenzene
A10847
1-Chloro-4-[(4-chlorophenyl)disulfanyl]benzene #
Q27284959
Z57056361
InChI=1/C12H8Cl2S2/c13-9-1-5-11(6-2-9)15-16-12-7-3-10(14)4-8-12/h1-8H