Lofroth, Goran et al. published their research in Acta Chemica Scandinavica (1947-1973) in 1967 | 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. Tetrahydropyrans and furans principally constitute as a central motif in diverse medicinally privileged molecules. There is large number of marine macrolide natural products that contain tetrahydropyran and tetrahydrofuran ring together. For instance, goniodomin A (actin targeting polyether), prorocentrolide (toxin halistatins), and percentotoxineRelated Products of 14431-43-7

Yields in the radiation degradation of solid carbohydrates was written by Lofroth, Goran. And the article was included in Acta Chemica Scandinavica (1947-1973) in 1967.Related Products of 14431-43-7 This article mentions the following:

The degradation induced by γ-irradiation of various simple polycrystalline carbohydrates has been studied by E.S.R. measurements of the solid samples, and by analyses of product formation and reactions occurring when the samples are dissolved in water. The area under the E.S.R. absorption curve is not inversely proportional to the absolute temperature at which the E.S.R. measurements are made, between 160 and 300°K., indicating a possible interaction between the radicals. When the irradiated carbohydrates are dissolved in water, they consume O that is dissolved in the water. It is postulated that radical-oxygen and radical-radical reactions are competitive. The consumption of dissolved O during the reaction was fit to an approx. equation from which the ratio of reaction velocities of radical-oxygen and radical-radical reactions was in the range of 10-15. The glucose(G) value of O consumption at high O concentrations of the water is 4 or higher. The aqueous solutions of the irradiated carbohydrates contain compounds, possibly organic peroxides, that oxidize ferrous ions of the FeSO4 reagent. The G value of ferrous ion oxidation is 4-10 for various carbohydrates. The yield of acids and the total degradation of the carbohydrates are strongly dependent on the crystalline form of the carbohydrate. 53 references. 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: 14431-43-7Related Products of 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. Tetrahydropyrans and furans principally constitute as a central motif in diverse medicinally privileged molecules. There is large number of marine macrolide natural products that contain tetrahydropyran and tetrahydrofuran ring together. For instance, goniodomin A (actin targeting polyether), prorocentrolide (toxin halistatins), and percentotoxineRelated Products of 14431-43-7

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