Can You Really Do Chemisty Experiments About 2,6-Di-O-methyl-β-cyclodextrin

Synthetic Route of 51166-71-3, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 51166-71-3.

New Advances in Chemical Research in 2021. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction by binding to a specific portion of an enzyme and thus slowing or preventing a reaction from occurring. 51166-71-3, Name is 2,6-Di-O-methyl-β-cyclodextrin, SMILES is COC[C@@H]1[C@]2([H])[C@@H]([C@@H](OC)[C@](O[C@]3([H])[C@H](O[C@@](O[C@]4([H])[C@H](O[C@@](O[C@]5([H])[C@H](O[C@@](O[C@@]6([H])[C@H](O)[C@@H](OC)[C@@](O[C@@H]6COC)([H])O[C@@]7([H])[C@H](O)[C@@H](OC)[C@@](O[C@@H]7COC)([H])O[C@@]8([H])[C@H](O)[C@@H](OC)[C@@](O[C@@H]8COC)([H])O2)([H])[C@H](OC)[C@H]5O)COC)([H])[C@H](OC)[C@H]4O)COC)([H])[C@H](OC)[C@H]3O)COC)([H])O1)O, in an article , author is Wu, Dao-Xin, once mentioned of 51166-71-3, Synthetic Route of 51166-71-3.

C16H14Cl2N2O5, monoclinic, P12(1)/cl (no. 14), a = 8.041(1) angstrom, b = 13.744(2) angstrom, c = 15.530(2) angstrom, beta = 100.201(2)degrees, V = 1689.2 angstrom(3), Z = 4, R-gt(F) = 0.044, wR(ref)(F-2) = 0.113, T = 298 K.

Synthetic Route of 51166-71-3, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 51166-71-3.

Reference:
1,3-Benzodioxole – Wikipedia,
,Dioxole | C3H4O2 – PubChem