Interesting scientific research on Mono-(6-p-toluenesulfonyl)-β-cyclodextrin

Synthetic Route of 67217-55-4, 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 67217-55-4.

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. 67217-55-4, Name is Mono-(6-p-toluenesulfonyl)-β-cyclodextrin, SMILES is O=S(OC[C@@H]1[C@@]([C@@H]([C@H]([C@]([H])(O1)O[C@@]23[H])O)O)([H])O[C@]4([H])[C@H](O)[C@H]([C@@]([H])([C@H](O4)CO)O[C@]5([H])[C@H](O)[C@H]([C@@]([H])([C@H](O5)CO)O[C@]6([H])[C@H](O)[C@H]([C@@]([H])([C@H](O6)CO)O[C@@]([H])(O[C@@H]([C@]7(O[C@@]([H])(O[C@@H]([C@]8(O[C@]([H])([C@@H]([C@H]2O)O)O[C@@H]3CO)[H])CO)[C@@H]([C@H]8O)O)[H])CO)[C@@H]([C@H]7O)O)O)O)O)(C9=CC=C(C=C9)C)=O, in an article , author is Wu, Dao-Xin, once mentioned of 67217-55-4, Synthetic Route of 67217-55-4.

Crystal structure of [3,4]dioxole-N ‘-(3,5-dichloro-2-hydroxybenzylidene)benzohydrazide – methanol (1:1), C15H10Cl2N2O4 center dot CH3OH

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 67217-55-4, 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 67217-55-4.

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