Interesting facts
Interesting Facts about 4-(4-nitrophenyl)sulfanylaniline
4-(4-nitrophenyl)sulfanylaniline is a fascinating compound that belongs to the class of anilines. This compound is notable for its unique structure and the various applications it has in the field of organic chemistry. Here are some intriguing points about this compound:
- Structural Significance: The presence of both a nitro group and a sulfanyl group significantly affects the compound's chemical properties and reactivity. The nitro group introduces electron-withdrawing characteristics while the sulfanyl group contributes nucleophilicity, which can lead to diverse reaction pathways.
- Applications in Synthesis: This compound serves as an important building block in organic synthesis. Its reactive sites allow it to participate in various reactions, making it useful for creating more complex organic molecules.
- Role in Analytical Chemistry: Compounds like 4-(4-nitrophenyl)sulfanylaniline are often employed in the development of sensor technologies and analytical methods. The absorption of light at specific wavelengths by the nitro group can be utilized in UV-Vis spectroscopy.
- Biological Importance: Some derivatives of sulfanylanilines demonstrate interesting biological activities, making this compound a relevant candidate in pharmaceutical research. It may open avenues toward the development of new drugs.
- Environmental Implications: The investigation of such compounds also raises awareness about their environmental impact due to their potential toxicity. Understanding their behavior in biological systems is crucial for assessing their environmental fate.
In summary, 4-(4-nitrophenyl)sulfanylaniline embodies the intricate balance of structural intricacy and functional potential. Its role in synthetic chemistry and biological applications, alongside its environmental significance, makes it a compound worthy of attention in the field of chemical sciences.
Synonyms
101-59-7
4-Amino-4'-nitrodiphenyl sulfide
4-((4-Nitrophenyl)thio)aniline
Benzenamine, 4-[(4-nitrophenyl)thio]-
4-(4-Nitrophenylthio)aniline
4-Aminophenyl 4-nitrophenyl sulfide
4-Amino-4'-nitrophenyl sulfide
4-(4-nitrophenyl)sulfanylaniline
4-(p-Nitrophenylthio)aniline
p-Aminophenyl p-nitrophenyl sulfide
4-Nitro-4'-aminophenyl sulfide
SULFIDE, ANILINO (p-NITROPHENYL)
4-Amino-4'-nitrodiphenyl thioether
p-((p-Nitrophenyl)thio)aniline
4-[(4-nitrophenyl)thio]aniline
NSC 23568
Benzenamine, 4-((4-nitrophenyl)thio)-
XZ6Y8J91OP
p-[(p-Nitrophenyl)thio]aniline
Aniline, p-((p-nitrophenyl)thio)-
Aniline, p-[(p-nitrophenyl)thio]-
NSC-23568
4-AMINO-4/'-NITRODIPHENYL SULFIDE
CCRIS 3894
EINECS 202-957-1
UNII-XZ6Y8J91OP
BRN 1882782
AI3-16817
4-amino-4'-nitrodiphenylsulfide
MFCD00007881
WLN: ZR DSR DNW
4-13-00-01292 (Beilstein Handbook Reference)
MLS000720145
SCHEMBL1713212
CHEMBL1352998
DTXSID6073154
p-(p-Nitrophenylmercapto)aniline
HMS2596P24
HMS3383N14
4-Amino-4'-nitrodiphenyl sulphide
NSC23568
4-[(4-Nitrophenyl)sulfanyl]aniline
4-Amino-4\'-Nitrodiphenyl Sulfide
STK257438
AKOS000108620
{4-[(4-nitrophenyl)thio]phenyl}amine
4-[(4-Nitrophenyl)sulfanyl]aniline #
4-Amino-4'-nitrodiphenyl sulfide, 98%
NCGC00245834-01
AC-10144
AS-14563
SMR000304674
AMINO-4'-NITROPHENYL SULPHIDE, 4-
A2077
NS00023072
D88505
SR-01000400164
SR-01000400164-1
Q27294067
Solubility of 4-(4-nitrophenyl)sulfanylaniline
The solubility of 4-(4-nitrophenyl)sulfanylaniline, a compound featuring both aromatic rings and a sulfonyl group, can be quite intriguing. Understanding its solubility characteristics is important for applications in various chemical processes. Here are some key points to consider:
In summary, the solubility of 4-(4-nitrophenyl)sulfanylaniline can be considered as a balance between its polar and non-polar characteristics, influenced by the choice of solvent, temperature, and pH. These factors play a crucial role in determining how this compound can be utilized in practical applications.