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N-desmethylclobenzorex

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Identification
Molecular formula
C15H20ClN
CAS number
2197-99-3
IUPAC name
2-chloro-N-ethyl-N-(1-naphthylmethyl)ethanamine
State
State
N-Desmethylclobenzorex is typically a solid at room temperature. It generally exists in a crystalline form, which can have significant implications for its solubility and absorption characteristics in various environments.
Melting point (Celsius)
80.20
Melting point (Kelvin)
353.40
Boiling point (Celsius)
305.60
Boiling point (Kelvin)
578.80
General information
Molecular weight
243.78g/mol
Molar mass
243.7630g/mol
Density
1.0378g/cm3
Appearence

N-Desmethylclobenzorex typically appears as a solid. It is often encountered in crystalline form and its color can range from white to off-white, depending on purity and specific conditions of synthesis.

Comment on solubility

Solubility Profile of 2-chloro-N-ethyl-N-(1-naphthylmethyl)ethanamine

The solubility of 2-chloro-N-ethyl-N-(1-naphthylmethyl)ethanamine is an intriguing factor in its chemical behavior and applications. This compound, with its unique molecular structure, exhibits solubility characteristics that are influenced by several factors:

  • Polarity: The presence of the chlorine atom and the ethyl group contributes to the overall polarity of the molecule. As a guideline, polar solutes tend to dissolve well in polar solvents, such as water.
  • Hydrophobic Nature of Naphthyl Group: The naphthyl part of the molecule is hydrophobic, which could limit its solubility in aqueous solutions but enhance it in organic solvents.
  • Temperature Dependency: As with many organic compounds, solubility may increase with temperature. Warmer environments can aid in breaking intermolecular interactions.
  • pH Influence: The solubility may also change with the pH of the solution, as the protonation state of amine functional groups can alter solubility.

In summary, the solubility of 2-chloro-N-ethyl-N-(1-naphthylmethyl)ethanamine can be considered moderate, with potential solubility in both organic solvents and a limited degree in water, depending on external conditions such as pH and temperature. Understanding these solubility dynamics is crucial for effectively utilizing this compound in various chemical processes and applications.

Interesting facts

Interesting Facts about 2-Chloro-N-ethyl-N-(1-naphthylmethyl)ethanamine

This compound is a fascinating example of a substituted amine, showcasing the complex interplay between aromatic systems and aliphatic chains in organic chemistry. Here are some key insights:

  • Structural Complexity: The compound features an ethyl group and a 1-naphthylmethyl group attached to a central ethanamine backbone. The presence of both aliphatic and aromatic components allows for unique reactivity and interactions essential in many biochemical processes.
  • Applications in Research: This compound is often studied for its potential applications in drug discovery. Compounds with naphthalene structures can serve as scaffolds for designing pharmacologically active agents due to their ability to mimic various biological interactions.
  • Toxicological Studies: The chlorinated derivative aspects of this compound raise interest in toxicology. Chlorinated compounds can exhibit unique toxicity profiles, prompting investigations into their environmental and health impacts.
  • Derivative Chemistry: The ability to modify this compound through substitution could lead to a myriad of derivatives, enhancing its utility in synthetic pathways within organic chemistry labs.
  • Analytical Techniques: Researchers often utilize techniques such as NMR and mass spectrometry to analyze such compounds. Understanding the structure-function relationship of 2-chloro-N-ethyl-N-(1-naphthylmethyl)ethanamine requires intricate analytical approaches for precise identification and characterization.

In summary, 2-chloro-N-ethyl-N-(1-naphthylmethyl)ethanamine serves as a remarkable case study for chemists interested in amine chemistry and its broader implications in medicinal chemistry and environmental science. Its rich structure and potential, coupled with ongoing research investigations, highlight the dynamic nature of this compound in contemporary chemical studies.

Synonyms
1-NAPHTHALENEMETHYLAMINE, N-(2-CHLOROETHYL)-N-ETHYL-
BRN 2726636
6470-73-1
N-(2-Chloroethyl)-N-ethylnaphthalene-1-methylamine
DTXSID60215032
DTXCID60137523
4-12-00-03193 (beilstein handbook reference)
AKOS012693617