Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition. 499-40-1, Name is (2R,3S,4R,5R)-2,3,4,5-Tetrahydroxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexanal, molecular formula is C12H22O11. In a Article，once mentioned of 499-40-1, Safety of (2R,3S,4R,5R)-2,3,4,5-Tetrahydroxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexanal
The copper(II) ion in the title complex, [Cu(C2H3O2)2-(C10H 9N3)].2H2O, is coordinated unsymmetrically to each of the two bidentate acetate ligands and to the N atoms of the di-2-pyridylamine (dpyam) ligand. The copper(II) ion is surrounded by a distorted square-based arrangement of the two dpyam pyridyl N atoms at distances of 1.974 (2) and 1.995 (2) A, and by two acetate O atoms at distances of 1.965 (1) and 1.967 (1) A. The second O atom from each acetate group is involved in weak coordination in the tetragonal positions, at longer Cu-O distances of 2.482 (2) and 2.690 (2) A, completing the six-coordination. The overall geometry at the copper(II) ion is best described as distorted octahedral with elongated axial bonds.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Safety of (2R,3S,4R,5R)-2,3,4,5-Tetrahydroxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexanal, you can also check out more blogs about499-40-1
Reference：
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics