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3-amino-N-ethyl-4-phenoxy-N-phenylbenzenesulfonamide

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Identification
Molecular formula
C20H20N2O3S
CAS number
66839-90-1
IUPAC name
3-amino-N-ethyl-4-phenoxy-N-phenyl-benzenesulfonamide
State
State

At room temperature, it is a solid.

Melting point (Celsius)
123.00
Melting point (Kelvin)
396.00
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.00
General information
Molecular weight
346.41g/mol
Molar mass
346.4140g/mol
Density
1.2400g/cm3
Appearence

The compound typically appears as a pale-yellow to off-white crystalline powder.

Comment on solubility

Solubility of 3-amino-N-ethyl-4-phenoxy-N-phenyl-benzenesulfonamide

The solubility of the compound 3-amino-N-ethyl-4-phenoxy-N-phenyl-benzenesulfonamide (C20H20N2O3S) can be considered a nuanced topic, primarily due to its varied interactions with different solvents. This compound has characteristics suggesting that it may have limited solubility in polar solvents like water, while showing better solubility in non-polar organic solvents.

Key Factors Influencing Solubility:

  • Hydrophobic Regions: The presence of phenyl groups in the structure can contribute to its hydrophobic nature.
  • Functional Groups: Although the amino and sulfonamide functional groups can engage in hydrogen bonding, they might not be enough to counterbalance the hydrophobic character.
  • Temperature: Solubility can also be temperature-dependent; higher temperatures may improve solubility in certain solvents.

To summarize, while 3-amino-N-ethyl-4-phenoxy-N-phenyl-benzenesulfonamide might exhibit limited water solubility, it could find better solubility profiles in organic mediums. Researchers should always perform empirical solubility tests to determine the best solvent environment for this compound.

Interesting facts

Interesting Facts about 3-amino-N-ethyl-4-phenoxy-N-phenyl-benzenesulfonamide

3-amino-N-ethyl-4-phenoxy-N-phenyl-benzenesulfonamide is a compound that showcases the fascinating intersection of organic chemistry and medicinal applications. Here are some intriguing aspects of this compound:

  • Versatile Structure: The compound features a complex molecular structure that includes an amino group, sulfonamide group, and a phenoxy group. This diversity in functional groups can lead to a range of biological activities, making it a subject of interest in drug design.
  • Potential Pharmaceutical Applications: Compounds with sulfonamide groups have historically been utilized in pharmaceuticals. The sulfonamide moiety is known for its antibacterial properties, which may lead to research into new antimicrobial agents.
  • Analytical Techniques: Studying such compounds often requires sophisticated analytical techniques like NMR (Nuclear Magnetic Resonance) spectroscopy and mass spectrometry. These methods help scientists unveil the compound's structure and confirm its purity.
  • Research Potential: Given its unique structure, researchers may explore derivatives of this compound to enhance its efficacy or reduce side effects, which underscores the importance of modifying chemical structures in drug development.
  • Interdisciplinary Collaboration: The study of compounds like 3-amino-N-ethyl-4-phenoxy-N-phenyl-benzenesulfonamide often necessitates collaboration between chemists, biologists, and pharmacologists, exemplifying the interdisciplinary nature of modern scientific research.

As we continue to explore the properties and applications of compounds such as this one, we gain insights into novel therapeutic strategies and deepen our understanding of the chemical principles that govern biological systems. This compound represents not only a chemical formula but also potential breakthroughs waiting to be discovered.

Synonyms
51929-55-6
3-amino-N-ethyl-4-phenoxy-N-phenylbenzenesulfonamide
EINECS 257-517-1
3-Amino-N-ethyl-4-phenoxy-N-phenylbenzenesulphonamide
MLS002695210
DTXSID60199888
NSC 93774
N'-Ethyl-4-phenoxymetanilanilide
NSC93774
CHEMBL1714608
DTXCID20122379
GHUSPTPILIZGPQ-UHFFFAOYSA-N
HMS3087C03
NSC-93774
AKOS024429051
SMR001561120
DB-294206
NS00032377
3-Amino-N-ethyl -4-phenoxy-N-phenylbenzenesulphonamide
257-517-1