Lee, Reiko T. published the artcileSynthesis of 3-(2-aminoethylthio)propyl glycosides, HPLC of Formula: 2595-07-5, the main research area is allyl alc glycoside addition; ethylthiopropyl glycoside; glucopyranoside ethylthiopropyl; galactopyranoside ethylthiopropyl.
Anomeric pairs of 3-(2-aminoethylthio)propyl D-galactopyranoside D-glucopyranoside and 2-acetamido-2-deoxy-D-glucopyranoside were prepared by addition of H2N(CH2)2SH to the corresponding anomeric allyl glycosides. The allyl α-glycosides were prepared by refluxing the sugars with allyl alc. in the presence of an acid catalyst; the allyl β-glycosides were prepared by the reaction of acetylated glycosyl bromides with allyl alc. in the presence of Hg(CN)2 followed by O-deacetylation. The rate of thiol addition to the allylic group was different for each glycoside.
Carbohydrate Research published new progress about Glycosides Role: SPN (Synthetic Preparation), PREP (Preparation). 2595-07-5 belongs to class alcohols-buliding-blocks, name is (2R,3R,4S,5R,6R)-2-(Allyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol, and the molecular formula is C9H16O6, HPLC of Formula: 2595-07-5.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts