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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
State
State

This compound is typically found as a liquid at room temperature, maintaining its liquid state across a moderate temperature range until reaching its relatively high boiling point.

Melting point (Celsius)
25.00
Melting point (Kelvin)
298.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
342.46g/mol
Molar mass
342.4620g/mol
Density
1.1000g/cm3
Appearence

This compound generally appears as a colorless or pale yellow liquid. It exhibits a faint, characteristic odor that is typical for amine-containing organic compounds.

Comment on solubility

Solubility of 2-(diethylamino)ethyl N-(3-butoxyphenyl)-N-phenyl-carbamate

Understanding the solubility of 2-(diethylamino)ethyl N-(3-butoxyphenyl)-N-phenyl-carbamate is key for its applications in various chemical processes and formulations. The solubility of this compound can be influenced by several factors, including:

  • Polarity: As a carbamate derivative, this compound is likely to exhibit moderate polarity due to the presence of functional groups, allowing it to dissolve in both polar and non-polar solvents to some extent.
  • Hydrogen Bonding: The ability to form hydrogen bonds with solvents may enhance its solubility in specific polar solvents like alcohols or dimethyl sulfoxide (DMSO).
  • Chain Length of Alkyl Groups: The diethylamino group and butoxyphenyl moiety can affect solubility. Generally, longer hydrocarbon chains tend to increase non-polar solvency but may decrease solubility in very polar environments.

It is essential to note that, while the solubility profile can provide insight into the compound's behavior in various mediums, empirical testing is often necessary to accurately determine the solubility in different solvents. As stated in chemical literature, "the solubility of a compound is a critical parameter that influences its bioavailability and functionality."

In practice, users can expect the compound to be soluble in:

  • Organic solvents like ethanol, acetone, and chloroform
  • Potentially less soluble in highly polar solvents such as water, hinting at limited aqueous solubility.

In conclusion, the solubility of 2-(diethylamino)ethyl N-(3-butoxyphenyl)-N-phenyl-carbamate is contingent upon various structural and environmental factors, making it a fascinating compound for further study.

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.

Synonyms
NIOSH/FD7642080
(m-Butoxyphenyl)phenylcarbamic acid 2-(diethylamino)ethyl ester
FD76420800
2-(Diethylamino)ethyl (m-butoxyphenyl)carbanilate
(m-Butoxyphenyl)carbanilic acid 2-(diethylamino)ethyl ester
Carbanilic acid, (m-butoxyphenyl)-, 2-(diethylamino)ethyl ester
Carbamic acid, (m-butoxyphenyl)phenyl-, 2-(diethylamino)ethyl ester