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N-ethyl-4-(4-nitrophenyl)sulfanyl-aniline

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Identification
Molecular formula
C14H14N2O2S
CAS number
N/A
IUPAC name
N-ethyl-4-(4-nitrophenyl)sulfanyl-aniline
State
State

At room temperature, N-ethyl-4-(4-nitrophenyl)sulfanyl-aniline is typically found as a solid. It is processed and stored under standard conditions in a stable crystalline form.

Melting point (Celsius)
158.50
Melting point (Kelvin)
431.65
Boiling point (Celsius)
479.15
Boiling point (Kelvin)
752.30
General information
Molecular weight
288.35g/mol
Molar mass
288.3460g/mol
Density
1.4256g/cm3
Appearence

N-ethyl-4-(4-nitrophenyl)sulfanyl-aniline typically appears as a pale yellow to yellow crystalline solid. The compound may also be in a powdered form, depending on its preparation and handling conditions.

Comment on solubility

Solubility of N-ethyl-4-(4-nitrophenyl)sulfanyl-aniline

N-ethyl-4-(4-nitrophenyl)sulfanyl-aniline presents unique characteristics regarding its solubility in various solvents:

  • Polar Solvents: This compound tends to be moderately soluble in polar solvents such as ethanol and methanol due to the presence of a polar amine group.
  • Apolar Solvents: Conversely, it exhibits lower solubility in non-polar solvents like hexane and cyclohexane because of its increased hydrophobic character.
  • pH Dependence: The solubility can also be influenced by pH levels. Under acidic conditions, protonation of the amine can enhance solubility.

In summary, the solubility of N-ethyl-4-(4-nitrophenyl)sulfanyl-aniline is shaped by its molecular structure, especially the balance of polar and non-polar functional groups. By adjusting the solvent type and conditions, chemists can optimize the solubility characteristics to achieve desired outcomes in various applications.

Interesting facts

Interesting Facts about N-ethyl-4-(4-nitrophenyl)sulfanyl-aniline

N-ethyl-4-(4-nitrophenyl)sulfanyl-aniline is a fascinating compound that straddles the intersection of organic chemistry and materials science. Here are some key points that highlight its significance and diverse applications:

  • Structural Diversity: This compound features a sulfonamide group and incorporates a nitrophenyl moiety, showcasing the complex interactions that can be engineered within aromatic systems.
  • Potential Applications: Due to its unique structure, this compound can serve as a precursor in the synthesis of various organic materials, including dyes and pharmaceuticals.
  • Biological Activity: Compounds containing nitro groups often exhibit *biological activities*, making them interesting candidates for further exploration in medicinal chemistry.
  • Chemical Reactions: The presence of the nitrophenyl group may influence the reactivity of the compound, enabling transformations that can lead to novel derivatives with tailored properties.

As noted by chemists, “the ability to modify molecular structures at the atomic level opens new avenues in synthesizing more effective materials.” This underscores the potential for N-ethyl-4-(4-nitrophenyl)sulfanyl-aniline to be pivotal in research and development across multiple scientific fields.

Such compounds remind us of the beauty and complexity of organic chemistry, where each unique molecular arrangement can lead to exciting discoveries and innovations!

Synonyms
5786-51-6
ANILINE, N-ETHYL-p-((p-NITROPHENYL)THIO)-
Benzenamine, N-ethyl-4-((4-nitrophenyl)thio)-
W3L4ET8V42
N-ethyl-4-(4-nitrophenyl)sulfanylaniline
BRN 3349140
p-Nitro-p'-ethylaminodiphenylsulfide
p-Nitro-p'-ethylaminodiphenylsulphide
N-Ethyl-p-((p-nitrophenyl)thio)aniline
UNII-W3L4ET8V42
DTXSID10206571
N-ETHYL-4-((4-NITROPHENYL)THIO)BENZENAMINE