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N,N-bis[(4-chlorophenyl)sulfanylmethyl]-4-methoxy-aniline

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Identification
Molecular formula
C20H17Cl2NO2S2
CAS number
59277-89-3
IUPAC name
N,N-bis[(4-chlorophenyl)sulfanylmethyl]-4-methoxy-aniline
State
State

At room temperature, N,N-bis[(4-chlorophenyl)sulfanylmethyl]-4-methoxy-aniline is found in the solid state, typically as a crystalline powder.

Melting point (Celsius)
151.50
Melting point (Kelvin)
424.65
Boiling point (Celsius)
653.00
Boiling point (Kelvin)
926.15
General information
Molecular weight
455.97g/mol
Molar mass
455.9710g/mol
Density
1.3640g/cm3
Appearence

This compound is a solid substance, typically appearing as a crystalline powder. The presence of the chlorophenyl groups offers a distinct yellowish to white color, and the compound may emit a faint aromatic odor due to its aromatic constituents.

Comment on solubility

Solubility of N,N-bis[(4-chlorophenyl)sulfanylmethyl]-4-methoxy-aniline

N,N-bis[(4-chlorophenyl)sulfanylmethyl]-4-methoxy-aniline is a complex organic compound that displays a nuanced solubility profile due to its molecular structure. Understanding its solubility is critical for various applications, including chemical synthesis and formulation chemistry.

Factors Influencing Solubility

  • Polarity: The presence of multiple aromatic rings and functional groups can influence the polarity of the compound. Polar solvents may enhance solubility, while non-polar solvents might be less effective.
  • Hydrogen Bonding: The -NH2 group can participate in hydrogen bonding, which may increase solubility in polar solvents like water.
  • Temperature: Solubility may increase with temperature, though this behavior can be specific to the solvent used.

Typically, compounds similar to N,N-bis[(4-chlorophenyl)sulfanylmethyl]-4-methoxy-aniline are more soluble in organic solvents (e.g., DMSO, acetone) compared to water. Thus, it is often necessary to evaluate solubility in context, testing various solvents to determine the best fit for specific applications.

Conclusion

In summary, while N,N-bis[(4-chlorophenyl)sulfanylmethyl]-4-methoxy-aniline may demonstrate limited solubility in water, it shows greater promise in organic solvents. As with many organic compounds, trial and error in solvent selection can yield optimal results for practical usage.

Interesting facts

Interesting Facts about N,N-bis[(4-chlorophenyl)sulfanylmethyl]-4-methoxy-aniline

N,N-bis[(4-chlorophenyl)sulfanylmethyl]-4-methoxy-aniline is a unique chemical compound with a variety of intriguing properties and potential applications. Here are some noteworthy points about this fascinating compound:

  • Complex Structure: The compound features a complex structure that includes aromatic rings and a sulfur linkage, hinting at interesting reactivity and biological activity.
  • Potential Biological Activity: The presence of chlorophenyl and aniline groups in its structure positions this compound as a candidate for exploration in the pharmaceutical field, particularly for its possible antibacterial or antifungal properties.
  • Synthetic Versatility: This compound can be synthesized using various chemical reactions, making it a valuable target for organic chemists aiming to develop new methodologies. The synthetic pathways often involve substitution reactions that showcase the reactivity of aromatic systems.
  • Research Opportunities: Due to the intriguing arrangement of its atoms, there is ample opportunity for research into its physical and chemical properties. Scientists are continually discovering how modifications to its structure can affect its functionality.
  • Applications in Material Science: The compound’s unique properties may also find applications in the development of new materials, potentially allowing for innovations in coatings, plastics, and other polymers.

In summary, N,N-bis[(4-chlorophenyl)sulfanylmethyl]-4-methoxy-aniline is more than just a chemical compound; it represents the intersection of synthetic chemistry, pharmacology, and material science. Its unique structure and potential applications make it an exciting topic for further research and exploration in the world of chemistry.

Synonyms
10381-05-2
NSC 89499
BRN 2782281
p-ANISIDINE, N,N-BIS(((p-CHLOROPHENYL)THIO)METHYL)-
N,N-Bis(((p-chlorophenyl)thio)methyl)-p-anisidine
DTXSID50146068
N,N-Bis[[(p-chlorophenyl)thio]methyl]-p-anisidine
DTXCID2068559
NSC89499
NSC-89499
WLN: GR DS1NR DO1&1SR DG
p-Anisidine,N-bis[[(p-chlorophenyl)thio]methyl]-