CAS 92621-31-3
:b-D-Mannopyranose,6-O-(triphenylmethyl)-, tetraacetate (9CI)
Description:
β-D-Mannopyranose, 6-O-(triphenylmethyl)-, tetraacetate (CAS 92621-31-3) is a derivative of the sugar mannose, specifically modified at the 6-position with a triphenylmethyl (trityl) group and acetylated at four hydroxyl groups. This compound is characterized by its pyranose ring structure, which is a six-membered ring containing five carbon atoms and one oxygen atom. The presence of the trityl group enhances the compound's stability and solubility in organic solvents, making it useful in various synthetic applications. The tetraacetate form indicates that all hydroxyl groups on the mannose are acetylated, which can influence the compound's reactivity and interactions in chemical reactions. This modification can also affect its biological properties, potentially impacting its use in biochemical studies or as a building block in carbohydrate chemistry. Overall, β-D-Mannopyranose, 6-O-(triphenylmethyl)-, tetraacetate is a valuable compound in organic synthesis and carbohydrate chemistry, providing insights into glycosylation reactions and the development of glycosyl donors.
Formula:C33H34O10
Synonyms:- Nsc52914
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Found 3 products.
1,2,3,4-Tetra-O-acetyl-6-O-trityl-β-D-mannopyranose
CAS:1,2,3,4-Tetra-O-acetyl-6-O-trityl-β-D-mannopyranoseMolecular weight:590.61705g/mol1,2,3,4-Tetra-O-acetyl-6-O-trityl-b-D-mannopyranose
CAS:1,2,3,4-Tetra-O-acetyl-6-O-trityl-b-D-mannopyranose is a synthetic sugar that can be used as a building block for the synthesis of oligosaccharides. It is also used to alter the properties of sugars and polysaccharides by modifying their glycosidic linkages. The product is insoluble in water and organic solvents. It is stable under acidic conditions and can be hydrolyzed with acids or alkalis. It is also soluble in methanol and methylene chloride. The CAS number for this product is 92621-31-3.End>Purity:Min. 95%
