Butoxycarbonyldiethylaminophenylethyl ether

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Identification

Molecular formula
C21H30N2O3
CAS Number
116-63-2
IUPAC Name
2-(diethylamino)ethyl N-(3-butoxyphenyl)-N-phenyl-carbamate
Molecular Weight
342.46g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1000g/cm3
Synonyms
NIOSH/FD7642080
Interesting facts

Interesting Facts about 2-(diethylamino)ethyl N-(3-butoxyphenyl)-N-phenyl-carbamate

2-(diethylamino)ethyl N-(3-butoxyphenyl)-N-phenyl-carbamate, often referred to as a carbamate derivative, is a fascinating compound with diverse applications in the field of medicinal chemistry. Below are some intriguing insights that highlight its significance:

  • Pharmaceutical Relevance: This compound plays a crucial role in the development of various pharmaceuticals, particularly as a potential candidate in processes that require selective pharmacological activity. Research has indicated that carbamate derivatives can exhibit significant anti-inflammatory and analgesic properties.
  • Mechanism of Action: The mode of action often involves the inhibition of specific enzymes or receptors within biological systems. Substituents such as the diethylamino group can enhance the lipophilicity of the compound, which often correlates with increased biological activity.
  • Structure-Activity Relationship (SAR): Understanding the SAR is essential for modifying this compound to enhance its efficacy. For example, the introduction of different aryl groups can lead to substantial changes in its biological profile. Researchers are continuously exploring how slight alterations can lead to better therapeutic outcomes.
  • Environmental Impact: The environmental significance of carbamates is noteworthy. Some derivatives can break down into less harmful components, making them subject to research on biodegradable pesticides and other agrochemicals.
  • Synthetic Pathways: The synthesis of this compound can involve various organic reactions, including esterification and amine nucleophilic substitution, showcasing an array of synthetic techniques that are critical for chemists to master.

In conclusion, the versatility and potential of 2-(diethylamino)ethyl N-(3-butoxyphenyl)-N-phenyl-carbamate make it a compound of considerable interest in both academic research and industrial applications. As science progresses, the avenues for its exploration will likely expand, placing it at the forefront of innovative medicinal chemistry.

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