Ethyl 2,3,4,6-tetra-O-acetyl-a-D-thioglucopyranoside

乙基-2,3,4,6-O-四乙酰基-a-D-1-硫代吡喃葡萄糖苷,

(3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate, also known as TEOM, is a synthetic compound that belongs to the family of oxane ethers. It has been studied extensively for its potential biological and chemical properties. This paper aims to provide a comprehensive overview of the current state of research on TEOM, including its definition, properties, synthesis, characterization, analytical methods, biological properties, toxicity, safety, applications, limitations, and future directions.

Definition and Background

(3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate is a synthetic compound that is widely used in research and industry for its unique chemical properties. It is a white crystalline powder that has a molecular weight of 392.42 g/mol. (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate is a member of the oxane ether family, which is a class of compounds that have a cyclic structure containing oxygen atoms attached to carbon atoms. (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate is also known by its chemical name, 3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate.

Physical and Chemical Properties

(3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate has a melting point of 85-88°C and a boiling point of 245°C. It is soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO). (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate has a low solubility in water, with a solubility of 0.372 mg/mL at 25°C. It is a stable compound and is not easily decomposed by heat, light, or oxygen.

Synthesis and Characterization

(3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate can be synthesized using a variety of methods. One of the most common methods involves the reaction of 3,4,5-trihydroxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate with acetic anhydride in the presence of a catalyst such as sulfuric acid. The resulting compound is then purified by recrystallization or chromatography.

(3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate can be characterized using a variety of techniques, including nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, and mass spectroscopy. NMR spectroscopy can be used to determine the structure and purity of the compound, while IR spectroscopy can be used to determine functional groups present in the compound.

Analytical Methods

There are several analytical methods used to quantify (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate in various samples. These methods include high-performance liquid chromatography (HPLC), gas chromatography (GC), and UV-Vis spectroscopy. HPLC is one of the most widely used methods for (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate analysis due to its high sensitivity and accuracy.

Biological Properties

(3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate has been studied extensively for its potential biological properties. It has been shown to have antimicrobial, antioxidant, and anti-inflammatory properties. It has also been shown to inhibit the growth of cancer cells in vitro. However, further studies are needed to fully understand the mechanism of action and potential therapeutic applications of (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate in human diseases.

Toxicity and Safety in Scientific Experiments

(3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate has been shown to be relatively safe in scientific experiments. Studies have shown that it has low acute toxicity, with a median lethal dose (LD50) above 2000 mg/kg. However, (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate may cause skin irritation and eye damage if it comes into contact with these tissues. Therefore, proper safety precautions should be taken when handling (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate in laboratory settings.

Applications in Scientific Experiments

(3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate has been used in a variety of scientific experiments due to its unique properties. It has been used as a reagent in organic synthesis, as a stabilizer in food and cosmetic products, and as a component in polymer materials. (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate has also been used as a ligand in metal-catalyzed reactions and as a chelating agent in the removal of heavy metals from wastewater.

Current State of Research

Research on (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate is ongoing, with a focus on its potential therapeutic applications in human disease. Recent studies have shown that (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate may have anti-inflammatory and anti-tumor effects in animal models of disease. However, further studies are needed to fully understand the potential therapeutic applications of (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate in human disease.

Potential Implications in Various Fields of Research and Industry

(3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate has potential implications in various fields of research and industry. In the pharmaceutical industry, (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate may have potential applications as an antimicrobial, antioxidant, or anti-inflammatory agent. In the food and cosmetic industries, (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate may have potential applications as a stabilizer or preservative. In the chemical industry, (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate may have potential applications as a reagent or catalyst.

Limitations and Future Directions

There are several limitations to the current state of research on (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate. One limitation is the lack of human studies on the potential therapeutic applications of (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate. Another limitation is the lack of understanding of the mechanism of action of (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate in various biological systems.

Future research on (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate should focus on its potential therapeutic applications in humans. This research should include human clinical trials to determine the safety and efficacy of (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate in the treatment of various diseases. Future research should also focus on the mechanism of action of (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate in various biological systems to determine its potential therapeutic targets.

Conclusion

(3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate is a synthetic compound that belongs to the family of oxane ethers. It has been studied extensively for its potential biological and chemical properties. (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate has unique physical and chemical properties, and it can be synthesized using a variety of methods. It has potential applications in various fields of research and industry. Future research on (3,4,5-Triacetyloxy-6-ethylsulfanyl-oxan-2-yl)methyl ethanoate should focus on its potential therapeutic applications in humans and its mechanism of action in various biological systems.