CAS 844877-56-1
:b-L-Xylofuranose, tetraacetate(9CI)
Description:
β-L-Xylofuranose, tetraacetate (9CI) is a synthetic carbohydrate derivative characterized by its furanose ring structure, which is a five-membered cyclic form of xylose. This compound features four acetyl groups attached to the hydroxyl groups of the xylofuranose, enhancing its stability and solubility in organic solvents. The presence of these acetyl groups also influences its reactivity, making it useful in various chemical reactions and applications, particularly in the field of organic synthesis and carbohydrate chemistry. The compound is typically utilized in research settings, including studies on glycosylation reactions and the development of glycosyl donors. Its molecular structure contributes to its unique properties, such as its ability to participate in specific interactions with biological molecules, which can be leveraged in drug design and development. As with many acetylated sugars, β-L-xylofuranose tetraacetate may exhibit different physical properties compared to its non-acetylated counterparts, including altered melting points and solubility profiles.
Formula:C13H18O9
Synonyms:- 1,2,3,5-Tetra-O-Acetyl-Beta-L-Xylofuranose
- 1,2,3,5-Tetra-O-Acetyl-Ss-L-Xylofuranose
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Found 3 products.
1,2,3,5-Tetra-O-acetyl-b-L-xylofuranose
CAS:1,2,3,5-Tetra-O-acetyl-b-L-xylofuranose is a carbohydrate. It is the only tetra-acetoxylated monosaccharide that has been reported to date. The synthesis of 1,2,3,5-tetra-O-acetyl-b-L-xylofuranose was achieved by modifying the glycosylation of bromoacetaldehyde with 1,2,3,5 triacetoxy xylan. This product has high purity and custom synthesis capabilities. It is also available as a methyl ether and can be modified using Click chemistry to incorporate different functional groups at specific positions on the molecule.Formula:C13H18O9Purity:Min. 95%Molecular weight:318.3 g/mol
