Interesting facts
Interesting Facts about 2-(2-hydroxyethylsulfanyl)-3-methyl-naphthalene-1,4-dione
2-(2-hydroxyethylsulfanyl)-3-methyl-naphthalene-1,4-dione, also known as a sulfonated naphthoquinone derivative, is a compound that showcases intriguing chemical properties and potential applications. Here are some fascinating insights:
- Unique Structure: The structure features a naphthalene core that is functionalized with hydroxyl and sulfhydryl groups. This combination adds significant chemical versatility, making the molecule of interest in organic synthesis.
- Biological Activity: Compounds derived from naphthoquinones have been studied for their biological properties. They exhibit activities such as anti-inflammatory, antimicrobial, and anticancer effects. This particular derivative’s unique substituents may enhance its bioactivity.
- Potential in Material Science: Research has shown that naphthoquinones can be utilized in the fabrication of organic electronic devices due to their conductive properties. The incorporation of sulfur groups may alter their electronic characteristics further.
- Analytical Relevance: 2-(2-hydroxyethylsulfanyl)-3-methyl-naphthalene-1,4-dione can be used as a marker in various chemical assays, particularly in studies involving redox reactions and electron transfer mechanisms.
- Environmental Applications: There is ongoing research into the applications of sulfur-containing compounds in environmental chemistry, especially in remediation technologies where they might play a role in detoxifying polluted environments.
In summary, 2-(2-hydroxyethylsulfanyl)-3-methyl-naphthalene-1,4-dione stands as a testament to the fascinating intersection of chemistry and various fields, from pharmacology to materials science. Its uniquely structured formula enhances its potential for various innovative applications.
Synonyms
59147-84-1
2-((2-Hydroxyethyl)thio)-3-methylnaphthalene-1,4-dione
2-(2-hydroxyethylthio)-3-methylnaphthalene-1,4-dione
2-[(2-Hydroxyethyl)thio]-3-methyl-1,4-naphthoquinone
NSC-672121
2-(2-hydroxyethylsulfanyl)-3-methylnaphthalene-1,4-dione
CHEMBL92659
2-[(2-Hydroxyethyl)thio]-3-methyl-1,4-naphthalenedione
2-[(2-Hydroxyethyl)thio]-3-methyl-1,4-napthalenedione
MFCD11100314
NSC672121
2-(2-hydroxyethylsulfanyl)-3-methyl-1,4-naphthoquinone
2-Hydroxyethylthio-3-methylnaphthoquinone
CPD 5 (pharmaceutical)
VK3-OH
SCHEMBL2599202
DTXSID50274390
GLXC-03008
BCP21745
BDBM50118676
AKOS016011513
NSC 672121
SMP2_000122
AC-37078
AS-69105
NCI60_025617
DB-009275
CS-0061155
I10534
2-(2-hydroxyethyl)thio-3-methyl-1,4-naphthoquinone
BRD-K55292075-001-01-0
2-(2-Hydroxy-ethylsulfanyl)-3-methyl-[1,4]naphthoquinone
2-[(2-HYDROXYETHYL)SULFANYL]-3-METHYLNAPHTHALENE-1,4-DIONE
2-[(2-hydroxyethyl)sulfanyl]-3-methyl-1,4-dihydronaphthalene-1,4-dione
Solubility of 2-(2-hydroxyethylsulfanyl)-3-methyl-naphthalene-1,4-dione
The compound 2-(2-hydroxyethylsulfanyl)-3-methyl-naphthalene-1,4-dione, with the chemical formula C12H10O3S, exhibits unique solubility characteristics that can be influenced by various factors. Understanding its solubility is essential for applications in pharmaceuticals and materials science.
Key Factors Affecting Solubility
Interestingly, solubility can also be described by the principle of like dissolves like. For 2-(2-hydroxyethylsulfanyl)-3-methyl-naphthalene-1,4-dione, its functional groups are crucial in determining compatibility with different solvent types. In applications, knowing that:
Ultimately, exploring the solubility of this compound is not just a matter of chemical properties; it is also vital for practical uses in formulations, ensuring optimal performance in intended applications. This highlights the importance of conducting solute-solvent interaction studies to harness the compound's potential effectively.