Skip to main content

N,N-bis(2-fluoroethyl)-4-[(4-methoxyphenyl)iminomethyl]aniline

ADVERTISEMENT
Identification
Molecular formula
C18H20F2N2O
CAS number
906341-21-5
IUPAC name
N,N-bis(2-fluoroethyl)-4-[(4-methoxyphenyl)iminomethyl]aniline
State
State

At room temperature, N,N-bis(2-fluoroethyl)-4-[(4-methoxyphenyl)iminomethyl]aniline is typically found as a solid. Its state can be described as crystalline, often forming as powder or small granules.

Melting point (Celsius)
109.00
Melting point (Kelvin)
382.15
Boiling point (Celsius)
430.20
Boiling point (Kelvin)
703.35
General information
Molecular weight
316.35g/mol
Molar mass
316.3470g/mol
Density
1.1930g/cm3
Appearence

N,N-bis(2-fluoroethyl)-4-[(4-methoxyphenyl)iminomethyl]aniline typically appears as a solid at room temperature. The compound can vary in color from off-white to yellowish, depending on its purity and the presence of any impurities. It is not hygroscopic and maintains its state under standard laboratory conditions.

Comment on solubility

Solubility of N,N-bis(2-fluoroethyl)-4-[(4-methoxyphenyl)iminomethyl]aniline

N,N-bis(2-fluoroethyl)-4-[(4-methoxyphenyl)iminomethyl]aniline exhibits unique solubility characteristics due to its complex molecular structure. Understanding these solubility traits is essential for various applications in chemical processes and formulations. Key points include:

  • Polar character: The presence of the fluoroethyl groups enhances the polar nature of the molecule, potentially increasing solubility in polar solvents.
  • Hydrophobic interactions: The methoxyphenyl substituent contributes to hydrophobic interactions, which can decrease solubility in highly polar solvents.
  • Solvent compatibility: It is likely to be more soluble in organic solvents such as dimethyl sulfoxide (DMSO) or acetone rather than in water.
  • Temperature dependency: Solubility may also be temperature-dependent, with increases in temperature possibly leading to better solubility.

In practical applications, understanding these aspects of solubility can facilitate effective formulation strategies and improve performance in various chemical contexts. As always, direct experimentation is invaluable for confirming solubility behavior in different media.

Interesting facts

Interesting Facts about N,N-bis(2-fluoroethyl)-4-[(4-methoxyphenyl)iminomethyl]aniline

This intriguing compound is a member of the aniline derivatives and exhibits a fascinating array of potential applications in the field of chemistry and material science. Here are some interesting points to consider:

  • Dual Functionality: The structure of N,N-bis(2-fluoroethyl)-4-[(4-methoxyphenyl)iminomethyl]aniline features both an amino group and a fluorinated side chain, which can lead to enhanced properties in various chemical reactions.
  • Photochemical Properties: The presence of the 4-methoxyphenyl group may contribute to interesting photochemical behaviors, making it a potential candidate for applications in fields such as organic electronics or photodynamic therapy.
  • Fluorine's Impact: Compounds containing fluorine often exhibit unique characteristics such as increased lipophilicity and improved metabolic stability. This can lead to better bioavailability in pharmaceuticals, making this compound noteworthy in medicinal chemistry.

As a scientist studying this compound, one might explore its potential for:

  1. Drug Development: The unique arrangement of functional groups might allow it to interact in novel ways with biological targets.
  2. Material Science: Investigating its use in developing advanced materials with specific desired properties due to the fluorinated components.
  3. Catalysis: The possibility of this compound serving as a catalyst or ligand in various chemical transformations is an exciting area for research.

In summary, N,N-bis(2-fluoroethyl)-4-[(4-methoxyphenyl)iminomethyl]aniline is a compound that carries the promise of innovation across multiple disciplines. Its structure holds secrets that could pave the way for advancements in pharmaceuticals, materials science, and beyond. Exploring this compound could lead to new discoveries that enhance our understanding of chemical interactions in diverse environments.

Synonyms
N-(p-(Bis(2-fluoroethyl)amino)benzylidene)-p-anisidine
4W4EGN5WM8
1237-83-8
p-ANISIDINE, N-(p-(BIS(2-FLUOROETHYL)AMINO)BENZYLIDENE)-
NSC-81714
NSC 81714
NSC81714
UNII-4W4EGN5WM8
NCIOpen2_009059
Benzenamine, N,N-bis(2-fluoroethyl)-4-[[(4-methoxyphenyl)imino]methyl]-
N,N-Bis(2-fluoroethyl)-4-[[(4-methoxyphenyl)imino]methyl]benzenamine