Interesting facts
Interesting Facts About 1-Nitro-4-phenylsulfanyl-benzene
1-Nitro-4-phenylsulfanyl-benzene, a fascinating compound, belongs to the class of nitro-substituted aromatic compounds. This compound features a unique arrangement that gives it distinct chemical properties and applications. Here are some intriguing facts:
- Versatile Applications: This compound is used in organic synthesis, particularly in the preparation of various drugs and dyes. Its aromatic character enhances its reactivity, making it valuable in developing pharmaceuticals.
- Structural Significance: The presence of the nitro group (-NO2) at the 1-position and phenylsulfanyl group (-SPh) at the 4-position creates a site of electronic differences within the molecule. This configuration can heavily influence the compound's reactivity and polarity.
- Electron-Withdrawing Properties: The nitro group is a strong electron-withdrawing group, making this compound an excellent candidate for nucleophilic substitution reactions. This property also affects its behavior in electrophilic aromatic substitution.
- Research Potential: Due to its unique structure, 1-nitro-4-phenylsulfanyl-benzene is of interest in medicinal chemistry. Researchers may explore its potential as an antibacterial or anticancer agent, making it a subject of ongoing studies.
- Environmental Impact: Like many organic compounds, it is crucial to assess the environmental effects of synthesis and degradation products. Understanding such compounds helps chemists design greener alternatives.
Overall, 1-nitro-4-phenylsulfanyl-benzene exemplifies the diversity of organic compounds and their potential in scientific research. With ongoing studies, it represents a bridge between fundamental chemistry and practical applications in a variety of fields.
Synonyms
4-Nitrophenyl phenyl sulfide
952-97-6
1-Nitro-4-(phenylsulfanyl)benzene
4-Nitrodiphenyl thioether
Phenyl-p-nitrophenyl sulfide
CCRIS 3887
EINECS 213-462-5
BRN 1912782
4-(Phenylthio)nitrobenzene
DTXSID50241784
4-06-00-01694 (Beilstein Handbook Reference)
4-NO2TE
DTXCID80164275
rjcbybqjvxvvkb-uhfffaoysa-n
4-Nitrodiphenyl sulfide
p-Nitrophenyl phenyl sulfide
(4-Nitrophenyl)(phenyl)sulfane
p-Nitrodiphenyl sulfide
Benzene, 1-nitro-4-(phenylthio)-
1-Nitro-4-(phenylthio)benzene
SULFIDE, p-NITROPHENYL PHENYL
Phenyl p-nitrophenylsulfide
1-nitro-4-phenylsulfanylbenzene
4-Nitrophenyl phenyl sulphide
NSC 87341
A6UNS7FMA7
1-nitro-4-phenylsulfanyl-benzene
NSC-87341
4-(nitrophenyl) phenyl sulphide
Benzene,1-nitro-4-(phenylthio)-
MFCD00024700
UNII-A6UNS7FMA7
NCIOpen2_005248
SCHEMBL268150
4-(Nitrophenyl) phenyl sulfide
NSC87341
4-Nitrophenyl phenyl sulfide, 97%
STK697629
AKOS005216932
AS-38165
DB-057573
CS-0204892
NS00040443
Solubility of 1-nitro-4-phenylsulfanyl-benzene
1-nitro-4-phenylsulfanyl-benzene, with its unique structure, presents interesting solubility characteristics. Understanding the solubility of this compound can be crucial for applications in chemical synthesis and formulation. Here are some key points:
In essence, while 1-nitro-4-phenylsulfanyl-benzene is not expected to be highly soluble in water, it may readily dissolve in various organic solvents, which is beneficial for its use in chemical processes. Always consider conducting solubility tests under controlled conditions for precise evaluation.