Chemoenzymic synthesis of 1′-photo-reactive sucrose derivatives via ether linkage was written by Tsunekawa, Yuka;Masuda, Katsuyoshi;Muto, Miho;Muto, Yasuyuki;Murai, Yuta;Hashidoko, Yasuyuki;Orikasa, Yoshitake;Oda, Yuji;Hatanaka, Yasumaru;Hashimoto, Makoto. And the article was included in Heterocycles in 2012.Reference of 126-14-7 This article mentions the following:
As the 1′-hydroxyl group of sucrose is well known to be less reactive than other primary alcs., there are no reports on the substitution of a phenoxy group at this position. Chemo-enzymic synthesis of photoreactive 1′-phenoxy-substituted sucrose was examined to elucidate the functional anal. of sweet receptors. In the experiment, the researchers used many compounds, for example, (2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(((2S,3S,4R,5R)-3,4-diacetoxy-2,5-bis(acetoxymethyl)tetrahydrofuran-2-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate (cas: 126-14-7Reference of 126-14-7).
(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(((2S,3S,4R,5R)-3,4-diacetoxy-2,5-bis(acetoxymethyl)tetrahydrofuran-2-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate (cas: 126-14-7) belongs to tetrahydrofuran derivatives.Tetrahydrofuran has many industry uses as a solvent including in natural and synthetic resins, high polymers, fat oils, rubber, polymer. Tetrahydrofuran (THF) is primarily used as a precursor to polymers including for surface coating, adhesives, and printing inks.Reference of 126-14-7
Referemce:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem