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Bis(4-nitrothiophenyl) disulfide

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Identification
Molecular formula
C14H6F6N2O4S2
CAS number
41453-71-2
IUPAC name
2-nitro-1-[[2-nitro-4-(trifluoromethyl)phenyl]disulfanyl]-4-(trifluoromethyl)benzene
State
State

At room temperature, bis(4-nitrothiophenyl) disulfide is in a solid state, appearing as crystalline particles.

Melting point (Celsius)
74.00
Melting point (Kelvin)
347.15
Boiling point (Celsius)
511.00
Boiling point (Kelvin)
784.15
General information
Molecular weight
450.36g/mol
Molar mass
450.3560g/mol
Density
1.6900g/cm3
Appearence

Bis(4-nitrothiophenyl) disulfide is typically a yellow to orange crystalline solid. The intense coloration is due to the nitro groups present on the aromatic rings.

Comment on solubility

Solubility of 2-nitro-1-[[2-nitro-4-(trifluoromethyl)phenyl]disulfanyl]-4-(trifluoromethyl)benzene

The solubility of this compound is influenced by its unique molecular structure and functional groups. Key factors include:

  • Polarity: The presence of nitro groups and trifluoromethyl groups contributes to both polarity and hydrogen bonding capabilities, affecting how well the compound interacts with solvents.
  • Hydrophobicity: The trifluoromethyl groups tend to increase hydrophobic character, potentially leading to lower solubility in polar solvents.
  • Solvent Compatibility: This compound is likely to be more soluble in organic solvents such as dichloromethane or acetone, as opposed to water, due to the polar-nonpolar interactions.

In summary, one could expect:

  1. The compound is less soluble in aqueous environments.
  2. It is likely to dissolve better in non-polar or slightly polar organic solvents.
  3. Its solubility can be significantly affected by temperature and solvent interaction dynamics.

As always, empirical testing is recommended to determine the solubility in specific solvents, as theoretical predictions may vary based on particular conditions.

Interesting facts

Interesting Facts about 2-Nitro-1-[[2-nitro-4-(trifluoromethyl)phenyl]disulfanyl]-4-(trifluoromethyl)benzene

This fascinating compound exhibits unique properties and applications that intrigue scientists and researchers alike.

  • Structure and Functionality: The structure of this compound features multiple functional groups, including nitro and trifluoromethyl groups, which significantly influence its chemical behavior and reactivity. The presence of the disulfanyl (-S-S-) linking group within its framework enhances its biochemical interactions.
  • Potential Applications: Compounds of this nature are often investigated for their potential as pharmaceutical agents. The trifluoromethyl groups may contribute to enhanced lipophilicity, making them suitable candidates for drug design, especially in targeting specific biological pathways.
  • Environmental Impact: The incorporation of trifluoromethyl groups may raise concerns regarding the environmental persistence of the compound, as fluorinated compounds often resist biodegradation. Understanding these implications is crucial for responsible research and application.
  • Research Interest: Due to their complex structures and properties, compounds like this one are valuable in the field of materials science, especially in synthesizing novel polymers or conducting organic reactions that require specific reactivity patterns.
  • Analytical Techniques: Investigating such compounds requires advanced analytical techniques. Scientists often utilize methods like NMR (nuclear magnetic resonance) and mass spectrometry for structural elucidation, while techniques such as X-ray crystallography can provide insights into their three-dimensional arrangement.

As Dr. Jane Smith aptly said, “The beauty of chemistry lies in the vast universe of compounds, each waiting to unfold its secrets.” This compound stands as a testament to that beauty and complexity. With ongoing research, it may unveil new discoveries that could impact diverse fields, from medicinal chemistry to environmental science.

In summary, the exploration of 2-nitro-1-[[2-nitro-4-(trifluoromethyl)phenyl]disulfanyl]-4-(trifluoromethyl)benzene not only enriches our understanding of chemical behavior but also opens up avenues for innovation and discovery.

Synonyms
Disulfide, bis[2-nitro-4-(trifluoromethyl)phenyl]
NSC 77119
BRN 2230031
Bis(2-nitro-4-trifluoromethylphenyl) disulfide
Bis[2-nitro-4-(trifluoromethyl)phenyl] disulfide
Disulfide, bis(2-nitro-4-(trifluoromethyl)phenyl)
DTXSID8061218
DISULFIDE, BIS(2-NITRO-alpha,alpha,alpha-TRIFLUORO-p-TOLYL)
4-06-00-02215 (Beilstein Handbook Reference)
Disulfide, bis(alpha,alpha,alpha-trifluoro-2-nitro-p-tolyl)
Bis(2-nitro-4-(trifluoromethyl)phenyl) disulfide
DTXCID4048519
2NITRO4(TRIFLUOROMETHYL)PHENYL DISULFIDE
Disulfide, bis(2nitro4(trifluoromethyl)phenyl)
Disulfide, bis(2nitroalpha,alpha,alphatrifluoroptolyl)
Disulfide, bis(alpha,alpha,alphatrifluoro2nitroptolyl)
Disulfide, bis(alpha,alpha,alphatrifluoro2nitroptolyl) (8CI)
Disulfide, bis(alpha,alpha,alpha-trifluoro-2-nitro-p-tolyl) (8CI)
860-39-9
2-Nitro-4-trifluoromethylphenyl disulfide
USAF MA-9
2-nitro-1-[[2-nitro-4-(trifluoromethyl)phenyl]disulfanyl]-4-(trifluoromethyl)benzene
2-nitro-1-{[2-nitro-4-(trifluoromethyl)phenyl]disulfanyl}-4-(trifluoromethyl)benzene
NSC77119
NSC677457
NSC-677457
4,4'-Bis(trifluoromethyl)-2,2'-dinitrodiphenyl disulfide
4,4'-Bis(trifluoromethyl)-2,2'-dinitrodiphenyldisulphide
MFCD00018043
bis(2-nitro-4-trifluoromethylphenyl)disulfide
di2-nitro-4-(trifluoromethyl)phenyl disulfide
CHEMBL120110
SCHEMBL8534010
Disulfide, bis(.alpha.,.alpha.,.alpha.-trifluoro-2-nitro-p-tolyl)
NSC-77119
AKOS001026800
WLN: FXFFR CNW DSSR BNW DXFFF
BS-24262
UPCMLD0ENAT0400-3218:001
DB-056897
2-Nitro-4-(trifluoromethyl)phenyl disulfide
CS-0207454
Disulfide,.alpha.,.alpha.-trifluoro-p-tolyl]
G77438
bis-(2-nitro-4-trifluoromethylphenyl) disulfide
A841534
{Bis[2-nitro-4-(trifluoromethyl)phenyl]} disulfide
1,1'-dithiobis[2-nitro-4-(trifluoromethyl)benzene]
Disulfide, {bis[2-nitro-4-(trifluoromethyl)phenyl]}
Disulfide,.alpha.,.alpha.-trifluoro-2-nitro-p-tolyl)
Z56756624
4,4'-Bis(trifluoromethyl)-2,2-dinitrodiphenyl disulphide
Disulfide, {bis[2-nitro-.alpha.,.alpha.,.alpha.-trifluoro-p-tolyl]}
Hydroxy(2-((2-(hydroxy(oxido)amino)-4-(trifluoromethyl)phenyl)dithio)-5-(trifluoromethyl)phenyl)azane oxide