Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice can avoid electrode passivation, which strongly inhibit the efficient activation of substrates. 14215-68-0, Name is N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide, molecular formula is C8H15NO6. In a Article，once mentioned of 14215-68-0, Application of 14215-68-0
Glucosamine analogues are inhibitors of yeast hexokinase (HK); kinetic analysis with respect to glucose and ATP suggests a pseudo-substrate behaviour for these compounds. However, a spectroscopy study by 31P NMR indicates that they are not phosphorylated but that, in fact, they enhance the ATPase activity of HK; this result gives a further insight into the phosphorylation or ATP hydrolysis process in HK.
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Reference：
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics