(1-ethylpyrrolidin-3-yl)methyl N-(2-chloro-6-methylphenyl)carbamate

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Identification

Molecular formula
C15H21ClN2O2
CAS Number
1189671-29-9
IUPAC Name
(1-ethylpyrrolidin-3-yl)methyl N-(2-chloro-6-methyl-phenyl)carbamate
Molecular Weight
294.80g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2300g/cm3
Synonyms
2-Chloro-6-methylcarbanilic acid (1-ethyl-3-pyrrolidinyl)methyl ester
Interesting facts

Interesting Facts about (1-ethylpyrrolidin-3-yl)methyl N-(2-chloro-6-methyl-phenyl)carbamate

(1-ethylpyrrolidin-3-yl)methyl N-(2-chloro-6-methyl-phenyl)carbamate is a fascinating compound with unique properties and potential applications. Here are some intriguing aspects to consider:

  • Chemical Structure: This compound consists of a pyrrolidine ring fused with a carbamate group, which plays a critical role in its biological activity.
  • Biological Relevance: Carbamates are often used in pharmacological settings. They can act as reversible inhibitors of enzymes, which is valuable in drug design.
  • Potential Applications: Due to its structural characteristics, this compound may have applications in areas such as:
    • Medications aimed at neurological disorders
    • Pest control products, given the effectiveness of carbamate derivatives in herbicides and insecticides
    • Research in organic chemistry for studying reaction mechanisms
  • Toxicological Studies: It's important to assess the toxicity profile of such compounds, particularly if they interact with biological systems.
  • The Role of Substituents: The presence of the chloro and methyl groups significantly influences the compound's reactivity and interaction with biological targets.

This compound serves as a prime example of how modifications in chemical structures can lead to diverse functionalities, opening a pathway for innovative research and potential therapeutic advances. As scientists continue to explore compounds like this one, the potential for discovery is vast and exciting!

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