Chlorphenesin carbamate
- Molecular formula
- C15H21ClN2O2
- CAS Number
- 886-74-8
- IUPAC Name
- 2-(1-piperidyl)ethyl N-(2-chloro-6-methyl-phenyl)carbamate
- Molecular Weight
- 316.80g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1680g/cm3
- Appearance
- can also vary slightly depending on the form in which it is prepared or processed for specific applications.
Identification
Interesting Facts about 2-(1-piperidyl)ethyl N-(2-chloro-6-methyl-phenyl)carbamate
This compound falls under the category of carbamates, which are notable for their diverse applications in both pharmaceuticals and agriculture. The structure of this compound features a piperidine ring, which contributes to its biological activity and significant pharmacological properties.
Key Features:
- Pharmacological Importance: Compounds similar to 2-(1-piperidyl)ethyl N-(2-chloro-6-methyl-phenyl)carbamate are often explored for their potential use as therapeutic agents, particularly in the field of neuroscience, due to their ability to modulate neurotransmitter activity.
- Environmental Relevance: As a carbamate, it may play a role in studies regarding agricultural chemistry where carbamates are commonly employed as pesticides, showcasing their importance in food production and pest management.
- Synthetic Routes: The synthesis of carbamates is a fascinating area of study, often involving reactions with isocyanates. This compound's synthesis may include steps that highlight the reactivity of amines and alcohols in organic chemistry.
- Structure-Activity Relationship: Understanding the relationship between the chemical structure and its biological activity can pave the way for the development of new drugs, making compounds like this one integral to medicinal chemistry.
The compound's name reveals a complex molecular architecture that suggests potential for specific interactions with biological targets. As a chemistry student or researcher, one can appreciate not just its functional groups, but also the intricate balance of chemical properties that make this compound both useful and interesting.
In summary, the exploration of 2-(1-piperidyl)ethyl N-(2-chloro-6-methyl-phenyl)carbamate opens doors to understanding the intricate world of carbamate chemistry and its critical role in modern science and technology.