Interesting facts
Interesting Facts about (2-Piperidin-1-ium-1-ylcyclohexyl) N-(2-chloro-6-methyl-phenyl)carbamate; Chloride
This compound represents a fascinating intersection of organic chemistry and medicinal science. Its complex structure showcases the ingenuity of synthetic methods in drug development. Here are some compelling aspects of this compound:
- Reactivity: The presence of the piperidinium moiety suggests that this compound could be highly reactive, allowing for interactions typical of quaternary ammonium compounds. This property is vital when designing pharmaceuticals as it can influence drug interactions and biological activity.
- Pharmacological Potential: Compounds featuring carbamate structures often exhibit biological activities. They are known to function as neuroprotective agents and may offer therapeutic benefits in treating various central nervous system disorders.
- Substituent Effects: The addition of a chloro and methyl substituent on the phenyl group can significantly alter the compound's properties. These effects can be strategically used to improve solubility, bioavailability, or specificity towards certain biological targets.
- Applications in Research: Due to its unique structure, researchers are exploring this compound's potential application in various fields, such as agrochemicals and antimicrobial agents. The wide range of applications reflects the versatility of carbamate derivatives.
- Synthesis and Complexity: Developing such intricate molecules is a testament to modern synthetic methodologies in organic chemistry. The synthetic pathways often involve multiple steps, showcasing the importance of strategic planning in the laboratory.
In summary, (2-Piperidin-1-ium-1-ylcyclohexyl) N-(2-chloro-6-methyl-phenyl)carbamate; chloride serves as a compelling example of how sophisticated organic compounds can integrate into drug discovery and development processes. Its structure not only encourages curiosity about its reactivity and potential uses but also pushes the boundaries of what is possible in chemical synthesis.
Synonyms
2-Chloro-6-methylcarbanilic acid 2-piperidinocyclohexyl ester hydrochloride
17095-85-1
K 1303
CARBANILIC ACID, 2-CHLORO-6-METHYL-, 2-PIPERIDINOCYCLOHEXYL ESTER, HYDROCHLORIDE
Carbanilic acid, 2-chloro-6-methyl-, 2-piperidinocyclohexyl ester, monohydrochloride
Solubility of (2-piperidin-1-ium-1-ylcyclohexyl) N-(2-chloro-6-methyl-phenyl)carbamate;chloride
The solubility of (2-piperidin-1-ium-1-ylcyclohexyl) N-(2-chloro-6-methyl-phenyl)carbamate;chloride is influenced by its structure and functional groups, which play a significant role in its interaction with solvents. Here are a few key points regarding its solubility:
In conclusion, the solubility of (2-piperidin-1-ium-1-ylcyclohexyl) N-(2-chloro-6-methyl-phenyl)carbamate;chloride is characterized by a complex interplay of chemical properties, making it essential to consider both the nature of the solvent and environmental conditions when assessing its solubility.