CAS 27821-11-0
:a-L-Mannopyranose, 6-deoxy-,1,2,3,4-tetraacetate
Description:
α-L-Mannopyranose, 6-deoxy-, 1,2,3,4-tetraacetate is a derivative of the sugar mannose, specifically modified by the acetylation of hydroxyl groups. This compound features a pyranose ring structure, which is a six-membered ring containing five carbon atoms and one oxygen atom. The "6-deoxy" designation indicates that the hydroxyl group at the sixth carbon has been removed, which alters its reactivity and biological properties. The tetraacetate form suggests that four hydroxyl groups have been acetylated, enhancing the compound's stability and solubility in organic solvents. This modification can also influence its interactions in biological systems, potentially affecting its role in glycosylation processes. The compound is typically used in biochemical research and synthesis, particularly in studies involving carbohydrate chemistry and the development of glycosylated compounds. Its CAS number, 27821-11-0, provides a unique identifier for regulatory and commercial purposes, facilitating its identification in chemical databases and literature.
Formula:C14H20O9
Synonyms:- Mannopyranose,6-deoxy-, tetraacetate, a-L- (8CI)
- a-L-Mannopyranose,6-deoxy-, tetraacetate (9CI)
- 1,2,3,4-Tetra-O-acetyl-a-L-rhamnopyranose
- Tetra-O-acetyl-a-L-rhamnopyranose
- Tetra-O-acetyl-a-L-rhamnose
- a-L-Rhamnopyranose tetraacetate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
1,2,3,4-Tetra-O-acetyl-a-L-rhamnopyranose
CAS:1,2,3,4-Tetra-O-acetyl-a-L-rhamnopyranose is a modified carbohydrate with the general structure of an oligosaccharide. It is a synthetic compound that has been modified with methylation and glycosylation. The purity of this product is high and it can be synthesized to order. This product has a CAS number of 27821-11-0 and can be found in the Carbohydrate section.Formula:C14H20O9Purity:Min. 95%Molecular weight:332.3 g/mol
