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N-(2-(2-(Diethylamino)ethoxy)ethyl)-4-chloroaniline

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Identification
Molecular formula
C14H23ClNO
CAS number
114649-96-2
IUPAC name
4-chloro-3-[2-[2-(diethylamino)ethoxy]ethyl]aniline
State
State

This compound is generally found in a liquid state at room temperature. It exhibits properties typical of many organic liquids, such as relatively low viscosity and volatility.

Melting point (Celsius)
-10.50
Melting point (Kelvin)
262.70
Boiling point (Celsius)
351.50
Boiling point (Kelvin)
624.70
General information
Molecular weight
256.79g/mol
Molar mass
256.7740g/mol
Density
1.0570g/cm3
Appearence

This compound typically appears as a colorless to pale yellow liquid. The exact shade can vary depending on the level of purity and specific form in which the compound is prepared.

Comment on solubility

Solubility of 4-chloro-3-[2-[2-(diethylamino)ethoxy]ethyl]aniline

The solubility of 4-chloro-3-[2-[2-(diethylamino)ethoxy]ethyl]aniline can be described as follows:

  • Solvent Dependency: The solubility of this compound is significantly influenced by the choice of solvent. It tends to dissolve more readily in polar solvents due to the presence of the diethylamino group, which can engage in hydrogen bonding.
  • Temperature Effects: Like many organic compounds, its solubility is likely to increase with temperature. Heating the solvent can often enhance the dissolution process, especially for compounds with larger molecular structures.
  • Concentration Limitations: In solution, this compound may exhibit saturation behavior. At high concentrations, the solubility may plateau making it less effective for certain applications.
  • Potential Applications: Its solubility characteristics can make it suitable for specific applications in medicinal chemistry, where solubility can impact bioavailability and therapeutic efficacy.

In summary, the solubility of 4-chloro-3-[2-[2-(diethylamino)ethoxy]ethyl]aniline is a multifaceted topic, with critical considerations for researchers looking to utilize its properties effectively. Always remember that "the solvent makes the solution!"

Interesting facts

Interesting Facts about 4-Chloro-3-[2-[2-(diethylamino)ethoxy]ethyl]aniline

This fascinating compound, commonly used in various chemical applications, has unique characteristics that make it a topic of interest in the field of chemistry. Here are some key points to note:

  • Functional Group Diversity: The compound contains multiple functional groups, including an aniline group and a chloro substituent. This rich variety allows for potential reactivity and a wide range of chemical behavior.
  • Biological Activity: Compounds with similar structures often exhibit significant biological activities. Research suggests that derivatives of 4-chloroaniline can exhibit antibacterial properties, making them valuable in pharmaceutical contexts.
  • Solvatochromic Properties: The presence of the diethylamino group hints at possible solvatochromic behavior, where color changes can occur in response to solvent polarity. This can be of interest in the design of sensors or indicators in chemical analysis.
  • Research Utility: This compound serves as a useful intermediate in the synthesis of more complex molecules, making it a valuable building block in organic chemistry. Its synthesis can provide insights into reaction mechanisms and synthetic pathways.

In summary, 4-chloro-3-[2-[2-(diethylamino)ethoxy]ethyl]aniline stands out not just as a chemical entity, but as a significant participant in the broader narrative of chemical research and application. Keep an eye on its developments, as it may reveal even more about the intersection of chemistry and biology!

Synonyms
26064-92-6
ANILINE, 4-CHLORO-3-(2-(2-(DIETHYLAMINO)ETHOXY)ETHYL)-
DTXSID30180703
RefChem:1070489
DTXCID30103194
4-Chloro-3-(2-(2-(diethylamino)ethoxy)ethyl)benzenamine
4-Chloro-3-(2-(2-(diethylamino)ethoxy)ethyl)aniline