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(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
State
State

At room temperature, this compound is typically found as a liquid.

Melting point (Celsius)
80.00
Melting point (Kelvin)
353.00
Boiling point (Celsius)
287.00
Boiling point (Kelvin)
560.00
General information
Molecular weight
294.80g/mol
Molar mass
294.7670g/mol
Density
1.2300g/cm3
Appearence

This compound appears as a colorless to pale yellow liquid, often used in research environments.

Comment on solubility

Solubility of (1-ethylpyrrolidin-3-yl)methyl N-(2-chloro-6-methyl-phenyl)carbamate

(1-ethylpyrrolidin-3-yl)methyl N-(2-chloro-6-methyl-phenyl)carbamate, a chemical characterized by its unique structure, demonstrates fascinating solubility properties that merit attention.

Generally, the solubility of organic compounds like this one can be influenced by several factors:

  • Polarity: The presence of functional groups such as carbamates can enhance solubility in polar solvents like water.
  • Hydrogen Bonding: The ability to form hydrogen bonds with solvents often correlates with increased solubility.
  • Molecular Size: Larger molecular structures might result in lower solubility due to steric hindrance.
  • Temperature: Typically, increasing temperature can increase solubility, especially for solid compounds.

When considering solubility, it is essential to recognize that:

  • The compound is likely to exhibit good solubility in organic solvents such as acetone or ethanol due to its hydrophobic characteristics.
  • Conversely, its solubility in water might be limited, indicating a complex interaction between its molecular structure and solvent properties.

In summary: While definitive solubility data may vary, understanding the interplay of structural elements facilitates predictions about solubility behavior. This compound exemplifies the nuanced solubility characteristics often encountered in organic chemistry.

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!

Synonyms
2-Chloro-6-methylcarbanilic acid (1-ethyl-3-pyrrolidinyl)methyl ester
20930-83-0
BRN 1484527
DTXSID10943217
CARBANILIC ACID, 2-CHLORO-6-METHYL-, (1-ETHYL-3-PYRROLIDINYL)METHYL ESTER
(1-Ethylpyrrolidin-3-yl)methyl hydrogen (2-chloro-6-methylphenyl)carbonimidate