Interesting facts
Interesting Facts About (2-nitrophenyl) thiohypochlorite
(2-nitrophenyl) thiohypochlorite is a fascinating compound that draws interest due to its unique chemical structure and properties. Here are some noteworthy aspects:
- Reactive Nature: This compound is known for its reactivity, particularly in *nucleophilic substitution reactions*. Its structure allows it to participate in various chemical transformations, making it a valuable reagent in organic synthesis.
- Applications in Synthesis: (2-nitrophenyl) thiohypochlorite can be utilized in the preparation of sulfur-containing compounds. Researchers often explore its potential in the development of *pharmaceuticals* and *agrochemicals*.
- Environmental Implications: As a chlorinated compound, its use raises questions about environmental impact. Understanding its degradation pathways can help in developing safer chemical processes.
- Structure-Activity Relationship: The presence of the nitro group enhances the electrophilic character of the aromatic system, influencing its reactivity. Analyzing such relationships is crucial in the field of *medicinal chemistry*.
- Safety Precautions: Working with (2-nitrophenyl) thiohypochlorite requires careful handling due to its *toxic and potentially hazardous* nature. Proper laboratory practices are essential to ensure safety.
In the world of synthetic organic chemistry, (2-nitrophenyl) thiohypochlorite stands out as an intriguing compound that continues to inspire research and innovation. As one scientist noted, "The beauty of chemistry lies in unraveling the secrets of seemingly simple compounds that hold the key to complex reactions."
Synonyms
2-Nitrobenzenesulfenyl chloride
7669-54-7
2-Nitrophenylsulfenyl chloride
Benzenesulfenyl chloride, 2-nitro-
o-Nitrobenzenesulfenyl chloride
O-NITROPHENYLSULFENYL CHLORIDE
Benzenesulfenyl chloride, o-nitro-
o-Nitrophenylsulphenyl chloride
o-Nitrobenzenesulphenyl chloride
EINECS 231-644-2
NSC 16179
2-nitrophenylsulphenyl chloride
DTXSID4064765
NPS-Cl
oNitrophenylsulfenyl chloride
2Nitrophenylsulfenyl chloride
oNitrobenzenesulfenyl chloride
oNitrophenylsulphenyl chloride
oNitrobenzenesulphenyl chloride
Benzenesulfenyl chloride, onitro
Benzenesulfenyl chloride, 2nitro
DTXCID9047912
Benzenesulfenyl chloride, onitro (8CI)
Benzenesulfenyl chloride, o-nitro-(8CI)
231-644-2
(2-nitrophenyl) thiohypochlorite
2-nitrophenyl hypochlorothioite
thiohypochlorous acid (2-nitrophenyl) ester
[(2-NITROPHENYL)SULFANYL]CHLORANE
MFCD00007128
NPS Reagent
2-nitrophenylthiochloride
nitrobenzene-sulfenyl chloride
2-nitrophenyl-sulfenylchloride
SCHEMBL397345
CS-M1921
NSC16179
NSC-16179
STL055641
AKOS005708612
AT23458
FS-3802
DB-021440
N0363
NS00037831
A838801
F0001-1957
InChI=1/C6H4ClNO2S/c7-11-6-4-2-1-3-5(6)8(9)10/h1-4
Solubility of (2-nitrophenyl) thiohypochlorite
(2-nitrophenyl) thiohypochlorite, a compound with a distinctive structure, exhibits specific solubility characteristics that play a significant role in its reactivity and application. Understanding its solubility can be key to manipulating its usage effectively.
Solubility Characteristics
The solubility of (2-nitrophenyl) thiohypochlorite can be influenced by various factors, and it is generally categorized as follows:
It is important to consider these factors together: solubility can significantly affect the stability and reactivity of (2-nitrophenyl) thiohypochlorite. As chemists often say, "Like dissolves like," emphasizing that compounds tend to dissolve in solvents with similar polar characteristics. Thus, for effective use and experimentation, understanding these solubility properties is crucial.