Synthesis of Novel Pyrazole-sucrose Derivatives by 1,3-dipolar Cycloaddition was written by Hajlaoui, Khaoula;El Guesmi, Ahlem;Ben Hamadi, Naoufel;Msaddek, Moncef. And the article was included in Journal of Heterocyclic Chemistry in 2018.COA of Formula: C12H20O6 This article mentions the following:
The syntheses of an important class of enantiopure five-membered glycoconjugates containing furan unit are described. The regioselective synthesis of a series of sugar-fused pyrazole heterocycles was achieved by the Huisgen cyclization of aryl diazomethanes with propargyl O-glycoside derivatives in good yields. The cycloaddition regioselectivity was confirmed by NMR. In the experiment, the researchers used many compounds, for example, (3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1COA of Formula: C12H20O6).
(3aS,4S,6R,6aS)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (cas: 14131-84-1) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Although benzodioxole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.COA of Formula: C12H20O6
Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem