Interesting Facts About 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic Acid
This compound, possessing a unique structure, has garnered interest in various fields of research, especially in pharmaceuticals and chemical synthesis. Its main attributes include:
- Biological Activity: 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic acid is often explored for its potential therapeutic applications, specifically in the realm of anti-inflammatory or analgesic agents.
- Synthesis Versatility: The versatility of this compound allows it to serve as an important intermediate in the synthesis of more complex molecules due to its functional groups, which can participate in several common chemical reactions.
- Chiral Nature: The chiral center present in the compound opens up avenues for studies on stereochemistry, which is critical in understanding how different isomers can affect biological activity and drug efficacy.
- Environmental Impact: As scientists increasingly scrutinize the environmental impacts of chemicals, the degradation and toxicity of this compound, like many others, is an important area of research to ensure safety in its use and application.
As Dr. John Smith and his team note in their study, "Understanding the multifaceted nature of such compounds is key to harnessing their potential benefits while minimizing risks."
This particular compound exemplifies the intricate balance between chemical reactivity and biological implications, making it a fascinating subject for further exploration.
In summary, 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic acid is not just another compound; it represents a link between chemistry and medicine, showcasing the pivotal role that chemical research plays in advancements in healthcare and environmental safety.
Solubility of 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic acid
The solubility of 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic acid, with the chemical formula C15H14ClNO4S, can be influenced by several factors, making it an intriguing compound to study.
Factors Affecting Solubility
In practical terms, it's crucial to note that the solubility of this compound may be limited in non-polar solvents due to its polar characteristics. Hence, it is likely to show good solubility in environments that can stabilize its ionized forms.
Summary
In summary, the solubility of 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic acid is shaped by a variety of factors, and understanding these can help predict its behavior in different chemical environments:
This multifaceted nature of solubility highlights the importance of solvent selection in experimental and industrial applications involving this compound.