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Diethylaminoethylmethylanthranilate

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Identification
Molecular formula
C17H26N2O3
CAS number
13444-24-5
IUPAC name
diethyl-[2-(3-hydroxy-4-methoxycarbonyl-anilino)-2-oxo-ethyl]-methyl-ammonium
State
State

At room temperature, this compound is in a liquid state.

Melting point (Celsius)
-16.00
Melting point (Kelvin)
257.20
Boiling point (Celsius)
371.60
Boiling point (Kelvin)
644.80
General information
Molecular weight
307.42g/mol
Molar mass
307.4210g/mol
Density
1.0400g/cm3
Appearence

This compound appears as a colorless to pale yellow liquid. It typically has a faint aromatic odor. The liquid is somewhat viscous in nature.

Comment on solubility

Solubility of Diethyl-[2-(3-hydroxy-4-methoxycarbonyl-anilino)-2-oxo-ethyl]-methyl-ammonium

Understanding the solubility characteristics of Diethyl-[2-(3-hydroxy-4-methoxycarbonyl-anilino)-2-oxo-ethyl]-methyl-ammonium is essential for its applications in various chemical processes. This compound displays interesting solubility traits that can be influenced by factors such as:

  • Polarity: Due to its ammonium group, this compound is expected to be more soluble in polar solvents like water, whereas it may exhibit lower solubility in non-polar solvents.
  • pH Levels: The solubility can vary with changes in pH, particularly because the ammonium group can become protonated, enhancing solubility in acidic conditions.
  • Temperature: An increase in temperature often increases solubility; thus, heating the solvent might enhance the dissolution of this compound.
  • Concentration: As with many chemical compounds, solubility can change with concentration, where higher concentrations may lead to saturation limits.

In practical terms, it is often observed that compounds similar to this one are soluble in aqueous environments due to their ionic character, making them suitable for biological or medicinal applications. However, if one seeks to utilize this compound in a particular solvent system, it’s crucial to conduct specific solubility tests to ascertain its behavior under desired conditions.

Ultimately, the solubility of Diethyl-[2-(3-hydroxy-4-methoxycarbonyl-anilino)-2-oxo-ethyl]-methyl-ammonium can be summarized succinctly: it is expected to be generally soluble in polar solvents and less soluble in non-polar ones, with further enhancements possible under favorable conditions.

Interesting facts

Interesting Facts about Diethyl-[2-(3-Hydroxy-4-methoxycarbonyl-anilino)-2-oxo-ethyl]-methyl-ammonium

This intriguing compound falls into the category of ammonium derivatives, which often display significant biological activity. The combination of diethyl and methyl groups with a complex aromatic structure suggests possible uses in medicinal chemistry, especially given the presence of an aniline component. Here are some noteworthy aspects:

  • Biological Significance: Compounds like this one, featuring nitrogen in a quaternary ammonium state, are often explored for their pharmacological properties. They can act as drug carriers or exhibit antimicrobial properties.
  • Structural Complexity: The presence of the 3-hydroxy-4-methoxycarbonyl group highlights how modifications to the aniline structure can lead to altered physicochemical properties and biological behaviors, making it a point of interest for drug design.
  • Synthetic Pathways: The synthesis of this compound may involve multi-step organic reactions, integrating various functional groups, which can be an engaging topic for chemistry students to explore the efficiency of synthetic routes.
  • Potential in Research: Researchers are likely inspired by the molecular architecture of this compound, as it could serve as a lead compound in the development of new therapeutic agents, particularly in combating drug-resistant pathogens.

This compound serves as a representation of how intricate molecular designs can lead to new discoveries in chemistry and medicine. As scientists continue to unravel the properties and applications of such compounds, they contribute vital knowledge that might advance the fields of organic chemistry and pharmacology.