Interesting facts
Interesting Facts about 2-(2,3-Dihydro-1,4-benzodioxin-6-yloxy)ethyl-methyl-ammonium Chloride
This compound, with its intricate structure, offers a fascinating exploration into the world of organic chemistry. Here are some key points to consider:
- Unique Structure: The compound contains a benzodioxin ring, which contributes to its chemical stability and reactivity. This part of the molecule plays a vital role in its biological interactions.
- Potential Applications: It has potential applications in medicinal chemistry, particularly in the development of new pharmaceuticals due to its ability to interact with biological systems.
- Quaternary Ammonium Salts: Being a quaternary ammonium compound, it exhibits properties typical of surfactants. These properties could be useful in developing agents for drug delivery or as disinfectants.
- Biological Relevance: Compounds like this one are often studied for their interactions with neurotransmitter systems, which can yield insights into treatments for neurological disorders.
As an organic chemist, one would appreciate the compound's balanced characteristics and functional groups, making it a prime candidate for further investigation. It serves as a testament to the diversity found in synthetic organic compounds and their potential roles in innovation and health.
In summary, 2-(2,3-dihydro-1,4-benzodioxin-6-yloxy)ethyl-methyl-ammonium chloride exemplifies the importance of understanding complex chemical entities in advancing both academic research and practical applications in various fields.
Synonyms
2-(1,4-Benzodioxan-6-yloxy)-N-methylethylamine hydrochloride
2906-76-5
ETHYLAMINE, 2-(1,4-BENZODIOXAN-6-YLOXY)-N-METHYL-, HYDROCHLORIDE
P-31
Solubility of 2-(2,3-dihydro-1,4-benzodioxin-6-yloxy)ethyl-methyl-ammonium;chloride
The solubility of the compound 2-(2,3-dihydro-1,4-benzodioxin-6-yloxy)ethyl-methyl-ammonium;chloride can be influenced by several factors:
In summary, it can be emphasized that the solubility of 2-(2,3-dihydro-1,4-benzodioxin-6-yloxy)ethyl-methyl-ammonium;chloride is primarily aided by its ionic nature, making it more favorable in polar environments such as water, while also remaining sensitive to factors like temperature and solvent choice. As the compound dissolves, it is not unusual to observe the release of chloride ions into solution, which can play a role in subsequent reactions or interactions.