Tabouret, Thierry et al. published their research in Comptes Rendus des Seances de l’Academie des Sciences, Serie C: Sciences Chimiques in 1980 | CAS: 14431-43-7

(2S,3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol hydrate (cas: 14431-43-7) belongs to tetrahydropyran derivatives. Numerous natural products have tetrahydropyran skeleton as the building block for designing new natural products and their derivatives e.g. aplysiatoxins, avermectins, oscillatoxins, talaromycins, latrunculins and acutiphycins. One classic procedure for the organic synthesis of tetrahydropyran is by hydrogenation of the 3,4-isomer of dihydropyran with Raney nickel.Recommanded Product: 14431-43-7

Fundamental study of honey and supersaturated glucose solution pasteurization was written by Tabouret, Thierry. And the article was included in Comptes Rendus des Seances de l’Academie des Sciences, Serie C: Sciences Chimiques in 1980.Recommanded Product: 14431-43-7 This article mentions the following:

The fundamentals of honey and supersaturated glucose [50-99-7] solution pasteurization (to prevent D-glucose monohydrate [14431-43-7] crystallization) were investigated by anal. ultracentrifugation, I.R and visible spectroscopy, and light and x-ray diffraction. Nonpasteurized solutions contained random clusters that were denser and more polydisperse than the surrounding medium, which is believed to consist only of more stable mol. associations as in well-pasteurized solutions In the experiment, the researchers used many compounds, for example, (2S,3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol hydrate (cas: 14431-43-7Recommanded Product: 14431-43-7).

(2S,3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol hydrate (cas: 14431-43-7) belongs to tetrahydropyran derivatives. Numerous natural products have tetrahydropyran skeleton as the building block for designing new natural products and their derivatives e.g. aplysiatoxins, avermectins, oscillatoxins, talaromycins, latrunculins and acutiphycins. One classic procedure for the organic synthesis of tetrahydropyran is by hydrogenation of the 3,4-isomer of dihydropyran with Raney nickel.Recommanded Product: 14431-43-7

Referemce:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics