Product Name:Ethyl 4,6-O-benzylidene-b-D-thioglucopyranoside
IUPAC Name:(4aR,6S,7R,8R,8aS)-6-(ethylsulfanyl)-2-phenyl-hexahydro-2H-pyrano[3,2-d][1,3]dioxine-7,8-diol
| Packing Unit | Available Stock | Price($) | Quantity |
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| CM182236-25g | in stock | ƏŁǎǎ |
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| Product Overview |
Ethyl 4,6-O-benzylidene-b-D-thioglucopyranoside (EBTG) is a synthetic compound that has been studied in both laboratory and clinical settings. It is a glycoside, a type of compound consisting of a sugar molecule linked to another molecule. In the case of EBTG, the sugar molecule is a thioglucose and the other molecule is an ethyl group. This compound has been studied for its potential applications in a variety of fields, including medicine and biochemistry. |
| Synthesis and Application |
Ethyl 4,6-O-benzylidene-b-D-thioglucopyranoside can be synthesized using a variety of methods. One of the most common methods is to use an acid-catalyzed reaction between ethyl 4-chlorobenzylidene-b-D-thioglucopyranoside and sodium ethoxide. This reaction produces a product with a yield of approximately 80%. Other methods, such as a reaction between ethyl 4-bromobenzylidene-b-D-thioglucopyranoside and sodium ethoxide, can also be used to synthesize Ethyl 4,6-O-benzylidene-b-D-thioglucopyranoside. Ethyl 4,6-O-benzylidene-b-D-thioglucopyranoside has been studied for its potential applications in a variety of scientific fields. In biochemistry, Ethyl 4,6-O-benzylidene-b-D-thioglucopyranoside has been used as a substrate for enzymes involved in the metabolism of carbohydrates and lipids. In medicine, Ethyl 4,6-O-benzylidene-b-D-thioglucopyranoside has been studied as a potential treatment for diabetes and other metabolic disorders. In addition, Ethyl 4,6-O-benzylidene-b-D-thioglucopyranoside has been studied as a potential inhibitor of the enzyme phosphodiesterase-4, which is involved in the regulation of inflammation. |
| Future Directions |
The potential applications of Ethyl 4,6-O-benzylidene-b-D-thioglucopyranoside are still being explored. Future research could focus on the development of more effective treatments for metabolic disorders and inflammation. In addition, further studies could be conducted to better understand the mechanisms of action of Ethyl 4,6-O-benzylidene-b-D-thioglucopyranoside and its effects on various biochemical and physiological processes. Finally, future studies could focus on the development of more efficient synthesis methods for Ethyl 4,6-O-benzylidene-b-D-thioglucopyranoside and other related compounds. |
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