New research progress on 51166-71-3 in 2021. Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. In an article, author is Walker, O, once mentioned the application of 51166-71-3, Reference of 51166-71-3, Name is 2,6-Di-O-methyl-β-cyclodextrin, molecular formula is C56H98O35, molecular weight is 1331.3563, MDL number is MFCD00011616, category is dioxole. Now introduce a scientific discovery about this category.
A medium size and rigid molecule (2,3-naphto-1,3-dioxole) has been selected for this study because full anisotropic reorientation is expected and because its symmetry elements dictate the orientation of the rotation-diffusion tensor. NMR measurements include direct cross-relaxation rates (which yield the three rotation-diffusion coefficients by assuming the length of CH bonds) and remote cross-relaxation rates (which, by using these rotation-diffusion coefficients, yield distances between a given carbon and remote protons). Two different solvents have been used: carbon disulfide and dimethyl sulfoxide, In both solvents, the same type of reorientation anisotropy is observed although with different ratios of rotation-diffusion coefficient values, presumably due to specific intermolecular interactions undergone by the dioxole ring. This would also explain geometrical variations at the level of this moiety. (C) 2002 Published by Elsevier Science B.V.
Reference of 51166-71-3, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 51166-71-3 is helpful to your research.
Reference:
1,3-Benzodioxole – Wikipedia,
,Dioxole | C3H4O2 – PubChem