(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. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.HPLC of Formula: 604-69-3
Synthesis of [15N4] purine labeled cytokinin glycosides derived from zeatins and topolins with 9-β-D, 7-β-D-glucopyranosyl, or 9-β-D-ribofuranosyl group was written by Tranova, Lenka;Bucek, Jan;Zatloukal, Marek;Cankar, Petr;Styskala, Jakub. And the article was included in Journal of Labelled Compounds and Radiopharmaceuticals in 2019.HPLC of Formula: 604-69-3 The following contents are mentioned in the article:
Synthesis of [15N4] purine labeled cytokinine glycosides derived from zeatins and topolins containing a 9-β-D-, 7-β-D-glucopyranosyl, or 9-β-D-ribofuranosyl group is described. These N6-substituted adenine derivatives are intended as internal analytic standards for phytohormone anal. All labeled compounds were prepared from 6-chloro[15N4]purine. The equilibrium reaction of 6-chloro[15N4]purine with acetobromo-α-D-glucose gave isomeric 7-β-D– and 9-β-D-chloro glucosyl precursors, which were treated with the corresponding amines to get desired labeled cytokinin 7-β-D– and 9-β-D-glucopyranosides. Cytokinins containing 9-β-D-ribofuranosyl group were obtained by direct enzymic transglycosylation reaction of cytokinins (7) prepared from 6-chloro[15N4] purine. 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. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.HPLC of Formula: 604-69-3
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics