Synthesis of trisaccharide repeating unit of fucosylated chondroitin sulfate was written by He, Haiqing;Chen, Dong;Li, Xiaomei;Li, Chengji;Zhao, Jin-Hua;Qin, Hong-Bo. And the article was included in Organic & Biomolecular Chemistry in 2019.HPLC of Formula: 604-69-3 The following contents are mentioned in the article:
We described the chem. synthesis of a sulfated trisaccharide repeating unit of fucosylated chondroitin sulfate (FCS), which has significant anticoagulant activity. Well-functionalized monosaccharides were readily prepared, and highly efficient glycosylation using a common activator (NIS/TfOH) were also presented. The synthesized trisaccharide could be used to extend oligosaccharide sequences. This study involved multiple reactions and reactants, such as (2S,3R,4S,5R,6R)-6-(Acetoxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate (cas: 604-69-3HPLC of Formula: 604-69-3).
(2S,3R,4S,5R,6R)-6-(Acetoxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate (cas: 604-69-3) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.HPLC of Formula: 604-69-3
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics