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1,4-Bis(p-nitrophenyl)thioether

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Identification
Molecular formula
C12H8N2O4S
CAS number
3955-40-6
IUPAC name
1-nitro-4-(4-nitrophenyl)sulfanyl-benzene
State
State

At room temperature, 1,4-Bis(p-nitrophenyl)thioether is in a solid state. It is typically handled as a crystalline powder for chemical processes and reactions.

Melting point (Celsius)
170.00
Melting point (Kelvin)
443.15
Boiling point (Celsius)
500.00
Boiling point (Kelvin)
773.15
General information
Molecular weight
308.33g/mol
Molar mass
308.3260g/mol
Density
1.4823g/cm3
Appearence

1,4-Bis(p-nitrophenyl)thioether appears as a yellow crystalline solid. Its crystalline nature allows for it to be distinguished from other similar compounds by its color and crystal structure.

Comment on solubility

Solubility of 1-nitro-4-(4-nitrophenyl)sulfanyl-benzene

The solubility of 1-nitro-4-(4-nitrophenyl)sulfanyl-benzene can be quite intriguing due to its unique chemical structure and properties. Here are some key points to consider:

  • Polar vs. Non-polar: This compound contains nitro groups, which are polar, suggesting the potential for some degree of solubility in polar solvents.
  • Solvent Compatibility: It may exhibit limited solubility in water due to its largely non-polar aromatic rings, but it could be more soluble in organic solvents such as:
    • Dimethyl sulfoxide (DMSO)
    • Acetone
    • Ethyl acetate
  • Temperature Effects: As with many organic compounds, increasing temperature may enhance solubility in organic solvents, making it easier to dissolve in higher concentrations.
  • Hydrogen Bonding: The presence of nitro groups might allow for hydrogen bond interactions with solvent molecules, potentially affecting solubility characteristics.

In conclusion, while 1-nitro-4-(4-nitrophenyl)sulfanyl-benzene may have limited solubility in water, it may show a more favorable solubility profile in various organic solvents. Further exploration into its solubility behavior can provide valuable insights into its applications and interactions in different environments.

Interesting facts

Exploring 1-nitro-4-(4-nitrophenyl)sulfanyl-benzene

1-nitro-4-(4-nitrophenyl)sulfanyl-benzene is a fascinating compound that draws interest not only for its unique structure but also for its potential applications in various fields of research. Here are some intriguing facts about this compound:

  • Structural Composition: This compound consists of a benzene ring with both nitro groups and a sulfanyl substituent, contributing to its multifaceted properties. The presence of multiple –NO2 groups can enhance reactivity and provides an interesting avenue for further chemical modifications.
  • Applications in Materials Science: Due to its unique electronic properties, 1-nitro-4-(4-nitrophenyl)sulfanyl-benzene can be utilized in the development of advanced materials such as conductive polymers or organic semiconductors.
  • Potential Antimicrobial Properties: Compounds with nitro and sulfanyl groups have been studied for their antimicrobial activities. This compound may hold promise for the development of novel antimicrobial agents, adding to its significance in medicinal chemistry.
  • Reactivity and Versatility: The nitro groups allow for various reactions such as reduction and nucleophilic substitution, which can be harnessed for synthesizing more complex molecules, making it a valuable intermediate in organic synthesis.
  • Research in Environmental Chemistry: The degradation and environmental impact of nitro compounds are of increasing concern. Studying 1-nitro-4-(4-nitrophenyl)sulfanyl-benzene can provide insights into the behavior of nitro compounds in various environmental contexts.

In conclusion, 1-nitro-4-(4-nitrophenyl)sulfanyl-benzene stands out not just for its chemical structure but also for its potential applications across various scientific disciplines. As researchers continue to explore its properties, this compound may uncover new pathways in both fundamental and applied chemistry.

Synonyms
Benzene, 1,1'-thiobis[4-nitro-
4-Nitrophenyl sulfide
4,4'-Dinitrodiphenyl sulfide
Bis(p-nitrophenyl)sulfide
Bis(4-nitrophenyl) sulphide
p,p'-Dinitrodiphenyl sulfide
Benzene, 1,1'-thiobis(4-nitro-
SULFIDE, BIS(p-NITROPHENYL)
NSC 11350
EINECS 214-950-0
BRN 2058966
1,1'-thiobis(4-nitrobenzene)
DTXSID9061629
1,1'-Thiobis[4-nitrobenzene]
DTXCID0033754
214-950-0
1223-31-0
Bis(4-nitrophenyl) Sulfide
Bis(4-nitrophenyl)sulfide
1-nitro-4-(4-nitrophenyl)sulfanylbenzene
1-Nitro-4-[(4-nitrophenyl)sulfanyl]benzene
di(p-Nitrophenyl) sulfide
MFCD00039745
H9L58S7KDK
4,4'-Dinitrodiphenylsulphide
NSC-11350
NSC629272
1-nitro-4-(4-nitrophenyl)sulfanyl-benzene
p-Nitrophenyl sulfide
dinitrodiphenyl sulfide
1-nitro-4-[(4-nitrophenyl)thio]benzene
4,4'-Dinitrophenylsulfide
Di(4-nitrophenyl) Sulfide
UNII-H9L58S7KDK
Sulphide, bis(p-nitrophenyl)
Benzene,1'-thiobis[4-nitro-
SCHEMBL4163474
ZZTJMQPRKBNGNX-UHFFFAOYSA-
NSC11350
AKOS001038321
NSC-629272
AS-60187
DB-041662
CS-0206171
D0847
NS00023986
EN300-17123
1-Nitro-4-[(4-nitrophenyl)sulfanyl]benzene #
D89728
Z56888735
Hydroxy(4-((4-(hydroxy(oxido)amino)phenyl)thio)phenyl)azane oxide
InChI=1/C12H8N2O4S/c15-13(16)9-1-5-11(6-2-9)19-12-7-3-10(4-8-12)14(17)18/h1-8H