Interesting facts
Interesting Facts About 2-Piperidin-1-ium-1-ylethyl N-(3-chloro-2-methyl-phenyl)carbamate; Chloride
2-Piperidin-1-ium-1-ylethyl N-(3-chloro-2-methyl-phenyl)carbamate; chloride is an intriguing compound that showcases the versatility of chemical structures and their applications. Here are some engaging insights:
- Pharmaceutical Relevance: This compound is often studied for its potential role in drug development and medicinal chemistry. The presence of the piperidine ring is significant as it is a common motif in many drugs, conferring favorable biological activity.
- Quaternization Effect: The quaternization of the piperidine nitrogen gives rise to cationic species, which can enhance the compound's interaction with biological membranes and improve its absorption and distribution.
- Chloro-Substituted Phenyl Ring: The presence of the 3-chloro-2-methyl-phenyl moiety adds chemical diversity and contributes to the compound’s reactivity profile, making it a subject of interest in synthetic organic chemistry.
- Functionality: The carbamate functional group plays a crucial role in the compound's behavior and stability. Carbamates are known for their activity in agrochemicals and could be explored for their potential in developing insecticides or herbicides.
- Synthetic Pathway: The synthesis of this compound may involve complex multi-step reactions, which allow chemists to explore various synthetic methodologies and reaction conditions.
According to chemists, "The beauty of compound design lies in the subtle balance of structure and function." This is particularly true for 2-piperidin-1-ium-1-ylethyl N-(3-chloro-2-methyl-phenyl)carbamate; chloride as researchers continue to unlock its potential.
In summary, this compound not only serves as a chemical curiosity but also opens doors to various applications across pharmaceuticals and agrochemicals, reflecting the dynamic interplay between structure, reactivity, and application in the field of chemistry.
Synonyms
3-Chloro-2-methylcarbanilic acid 2-piperidinoethyl ester hydrochloride
20224-18-4
K 442
CARBANILIC ACID, 3-CHLORO-2-METHYL-, 2-PIPERIDINOETHYL ESTER, HYDROCHLORIDE
Solubility of 2-piperidin-1-ium-1-ylethyl N-(3-chloro-2-methyl-phenyl)carbamate;chloride
The solubility of 2-piperidin-1-ium-1-ylethyl N-(3-chloro-2-methyl-phenyl)carbamate;chloride can be influenced by several factors, primarily its ionic nature and the presence of specific functional groups.
Generally, compounds containing quaternary ammonium structures, like this one, exhibit good solubility in polar solvents due to their ionic character. Here are a few key points to consider:
In summary, while the compound is expected to be soluble in polar solvents, particularly water, the exact solubility can still be influenced by temperature and the specific solvent characteristics used in applications. “Ionic character” plays a significant role in determining solubility, making this aspect crucial for practical utilizations.