Nombre del producto: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

CAS:20701-61-5
Fórmula molecular:C15H20O5S
Pureza:97%
Número de catálogo:CM182236
Peso molecular:312.38

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Detalles del producto

Núm. De CAS :20701-61-5
Fórmula molecular:C15H20O5S
Punto de fusión:-
Código de sonrisas:O[C@H]([C@H]([C@@H]([C@@H](CO1)O2)OC1C3=CC=CC=C3)O)[C@@H]2SCC
Densidad:
Número de catálogo:CM182236
Peso molecular:312.38
Punto de ebullición:
Nº Mdl:
Almacenamiento:

Category Infos

Carbohydrates
Carbohydrates are polyhydroxy aldehydes (aldoses) or polyhydroxy ketones (ketoses) composed of C, H and O, or form polyhydroxy aldehydes or ketones upon hydrolysis. Carbohydrates come in the form of monosaccharides, disaccharides, oligosaccharides and polysaccharides. The simplest sugars, monosaccharides and disaccharides, consist of one or two monosaccharide units. Oligosaccharides are generally classified as carbohydrates containing 3-10 monosaccharide units. Polysaccharides contain more than 10 monosaccharide units and can be quite large. Glucose is an aldose, the most important monosaccharide in the body, used by cells as fuel. Other aldohexoses are galactose and mannose, which form part of complex molecules. Fructose is a ketohexose sugar, while ribose is the most important aldose pentose sugar and a component of RNA.
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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.