Interesting facts
Exploring 2-[4-(4-aminophenyl)sulfonylanilino]ethanol
The compound 2-[4-(4-aminophenyl)sulfonylanilino]ethanol is an intriguing molecule with noteworthy characteristics. As a scientist or a chemistry student, one can appreciate the following aspects of this compound:
- Structure and Composition: This compound features a sophisticated arrangement involving a sulfonyl group, which enhances its potential functionality in various chemical reactions. The presence of an amino group contributes to its basic properties, making it a potential candidate for reactions where amines are involved.
- Applications in Medicine: Compounds like this one can be significant in medicinal chemistry. They may have applications in the developement of pharmaceuticals, especially in the development of anti-inflammatory or analgesic drugs.
- Research Significance: Scientists are often interested in compounds with sulfonamide groups due to their bioactivity. The unique arrangement of functional groups within this molecule allows for the investigation of its interactions with biological systems.
- Diverse Reactions: The amino and hydroxyl groups in this compound can participate in a variety of chemical reactions, including amination, nitration, and condensation reactions, which makes it a versatile compound for synthetic chemists.
- Cultural Chemistry: The “sulfonamides” have historical significance as one of the first classes of antibiotics. Studying such compounds can lead to advances in treatments and understanding of bacterial resistance.
As you delve into the unique properties and potential applications of 2-[4-(4-aminophenyl)sulfonylanilino]ethanol, you may find it offers endless opportunities for exploration and innovation within the realm of chemistry. This compound exemplifies how even the most specific chemical structures can play a vital role in diverse scientific fields.
Synonyms
Smith's sulfone
2-(4-Sulfanilylanilino)ethanol
Proethyl
2-p-Sulfanilylanilinoethanol
80-02-4
2-(p-Sulfanilylanilino)ethanol
ETHANOL, 2-(p-SULFANILYLANILINO)-
2-[4-(4-aminophenyl)sulfonylanilino]ethanol
NSC 12982
BRN 3059614
UNII-2G7D83186S
NSC-12982
NSC-30452
4-Amino-4'-beta-hydroxyethylamino diphenylsulfone
2G7D83186S
2-[[4-[(4-Aminophenyl)sulfonyl]phenyl]amino]ethanol
Ethanol, 2-((4-((4-aminophenyl)sulfonyl)phenyl)amino)-
DTXSID40229990
4-13-00-01326 (Beilstein Handbook Reference)
2-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)ethanol
4-Amino-4'-(.beta.-hydroxyethylamino)diphenyl sulfone
2-P-SULFANILYLANILINOETHANOL [MI]
2-(P-(P-AMINOPHENYLSULFONYL)PHENYL)AMINO)ETHANOL
4-Aminophenyl-4'-[.beta.-hydroxyethylaminophenyl]sulfone
Ethanol, 2-[[4-[(4-aminophenyl)sulfonyl]phenyl]amino]-
4-Amino-4'-(beta-hydroxyethylamino)diphenyl sulfone
SCHEMBL1042560
CHEMBL4636768
DTXCID90152481
NSC12982
NSC30452
AKOS024332549
2-(4-[(4-Aminophenyl)sulfonyl]anilino)ethanol #
4-Aminophenyl-4'-(beta-hydroxyethylaminophenyl)sulfone
Q27254703
622-300-6
Solubility of 2-[4-(4-aminophenyl)sulfonylanilino]ethanol
The solubility of 2-[4-(4-aminophenyl)sulfonylanilino]ethanol in various solvents is quite intriguing and plays a vital role in its application and function. This compound can be analyzed by considering several factors:
Considering the interactions at play, it's essential to remember that “like dissolves like”; thus, polar solvents will facilitate solubility due to the polar nature of the compound, while non-polar solvents may hinder it. The compound's unique structure emphasizes the complex nature of solubility, which can influence its reactivity and utility in various chemical processes.
In summary, while 2-[4-(4-aminophenyl)sulfonylanilino]ethanol may display moderate solubility in water, its compatibility with organic solvents highlights its versatility, making it an interesting subject for further exploration in solubility dynamics.