CAS 92051-25-7
:2-S-β-<span class="text-smallcaps">D</smallcap>-Glucopyranosyl-2-thio-<smallcap>D</span>-glucose
Description:
2-S-β-D-Glucopyranosyl-2-thio-D-glucose, with the CAS number 92051-25-7, is a thio-derivative of glucose that features a sulfur atom in place of an oxygen atom in the glycosidic bond. This compound is characterized by its glycosidic linkage, which connects a glucose unit to a thio-glucose moiety, imparting unique chemical properties compared to its oxygen-containing counterparts. The presence of the sulfur atom can enhance the compound's stability and reactivity, making it of interest in various biochemical applications. It may exhibit different solubility characteristics in polar solvents due to the thioether functionality. Additionally, this compound can participate in redox reactions, potentially serving as a reducing agent. Its structural features may also influence its biological activity, making it relevant in studies related to carbohydrate chemistry and potential therapeutic applications. Overall, 2-S-β-D-Glucopyranosyl-2-thio-D-glucose represents a fascinating area of study within the realm of modified carbohydrates.
Formula:C12H22O10S
InChI:InChI=1S/C12H22O10S/c13-1-4(16)7(17)9(19)6(3-15)23-12-11(21)10(20)8(18)5(2-14)22-12/h3-14,16-21H,1-2H2/t4-,5-,6+,7-,8-,9-,10+,11-,12+/m1/s1
InChI key:InChIKey=KDQJDKCXLOKGBA-VDONBHLQSA-N
SMILES:S([C@H]([C@H]([C@@H]([C@@H](CO)O)O)O)C=O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Synonyms:- Thiosophorose
- 2-S-β-D-Glucopyranosyl-2-thio-D-glucose
- D-Glucose, 2-S-β-D-glucopyranosyl-2-thio-
- 2-S-beta-D-Glucopyranosyl-2-thio-D-glucose
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Found 1 products.
Thiosophorose
CAS:<p>Thiosophorose is a nutrient that is found in microalgae. It is also known as d-arabinose and has been shown to be an inactivating agent for viruses, such as HIV-1. Thiosophorose has been used in skin care products due to its ability to produce fatty acids, which are important for healthy skin. It is also useful for the production of biofuels from microalgae. This molecule can be used to catalyze the reaction between amines and triflates and it is insoluble in water. The viscosity of this compound will increase with increasing temperature.</p>Formula:C12H22O10SPurity:Min. 95%Molecular weight:358.4 g/mol
