Interesting facts
Interesting Facts about [4-(1-allylbut-3-enyl)phenyl]ammonium Chloride
[4-(1-allylbut-3-enyl)phenyl]ammonium chloride is a fascinating compound that showcases the intricate relationship between organic structures and their applications in various fields. Here are some intriguing aspects of this compound:
- Unique Structure: This compound features a distinctive phenyl group that is substituted at the para position by a complex alkyl chain. This structural arrangement can influence the compound's chemical reactivity and biological properties.
- Potential Uses: Compounds similar to this ammonium salt are often researched for their potential use as ionic liquids, catalysts in organic synthesis, or as intermediates in the production of pharmaceuticals due to their unique solubility properties.
- Biological Interest: The presence of the phenyl group combined with the ammonium functionality can contribute to biological activity, making such compounds valuable for medicinal chemistry and drug design.
- Functional Versatility: The allylic chain in this compound opens avenues for further chemical modifications, allowing scientists to explore a variety of derivatives with enhanced or altered properties.
- Research Opportunities: Due to its unique characteristics, [4-(1-allylbut-3-enyl)phenyl]ammonium chloride presents numerous opportunities for research focusing on organic synthesis, material science, and even medicinal applications.
In conclusion, this compound not only has a complex and interesting structure but also represents a gateway to numerous applications in science and industry. As researchers continue to explore and manipulate such ammonium salts, we may uncover new materials or treatments that could impact various scientific domains.
As the great chemist Linus Pauling once said, "Science is the search for truth." Discovering the truths behind compounds like this one adds to our ever-growing understanding of chemistry!
Synonyms
Diallyl-p-aminophenylmethane hydrochloride
13064-22-7
p-(1-Allyl-3-butenyl)aniline hydrochloride
ANILINE, p-(1-ALLYL-3-BUTENYL)-, HYDROCHLORIDE
Solubility of [4-(1-allylbut-3-enyl)phenyl]ammonium chloride
The compound [4-(1-allylbut-3-enyl)phenyl]ammonium chloride (C13H18ClN) exhibits some intriguing solubility characteristics that are worthy of exploration.
Typically, ionic compounds tend to have higher solubility in polar solvents compared to nonpolar ones. In this case, the presence of the ammonium group, which is positively charged, indicates that this compound is likely to be soluble in water due to:
However, the solubility may also be influenced by:
In practice, it is essential to carefully consider the solvent environment when assessing the solubility of [4-(1-allylbut-3-enyl)phenyl]ammonium chloride. As a general observation, while ionic compounds like this one tend to be more soluble in polar environments, the balance between hydrophilic and hydrophobic components can significantly dictate the overall solubility behavior.
In conclusion, while the statement "soluble in water" might hold true for [4-(1-allylbut-3-enyl)phenyl]ammonium chloride, it is crucial to conduct empirical studies to determine precise solubility values across different temperatures and concentrations.