Flexible application of in synthetic route 82954-65-2

In addition to the literature in the link below, there is a lot of literature about this compound((S)-(2,2-dimethyl-[1,3]-dioxolan-4-yl)-methylamine)Reference of (S)-(2,2-dimethyl-[1,3]-dioxolan-4-yl)-methylamine, illustrating the importance and wide applicability of this compound(82954-65-2).

Reference of (S)-(2,2-dimethyl-[1,3]-dioxolan-4-yl)-methylamine. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: (S)-(2,2-dimethyl-[1,3]-dioxolan-4-yl)-methylamine, is researched, Molecular C6H13NO2, CAS is 82954-65-2, about Stereochemistry-Controlled Supramolecular Architectures of New Tetrahydroxy-Functionalized Amphiphilic Carbocyanine Dyes. Author is Schade, Boris; Singh, Abhishek Kumar; Wycisk, Virginia; Cuellar-Camacho, Jose Luis; von Berlepsch, Hans; Haag, Rainer; Boettcher, Christoph.

The syntheses of novel amphiphilic 5,5′,6,6′-tetrachlorobenzimidacarbocyanine (TBC) dye derivatives with aminopropanediol head groups, which only differ in stereochem. (chiral enantiomers, meso form and conformer), are reported. For the achiral meso form, a new synthetic route towards asym. cyanine dyes was established. All compounds form J aggregates in water, the optical properties of which were characterized by means of spectroscopic methods. The supramol. structure of the aggregates is investigated by means of cryo-transmission electron microscopy, cryo-electron tomog. and AFM, revealing extended sheet-like aggregates for chiral enantiomers and nanotubes for the mesomer, resp., whereas the conformer forms predominately needle-like crystals. The experiments demonstrate that the aggregation behavior of compounds can be controlled solely by head group stereochem., which in the case of enantiomers enables the formation of extended hydrogen-bond chains by the hydroxyl functionalities. In case of the achiral meso form, however, such chains turned out to be sterically excluded.

In addition to the literature in the link below, there is a lot of literature about this compound((S)-(2,2-dimethyl-[1,3]-dioxolan-4-yl)-methylamine)Reference of (S)-(2,2-dimethyl-[1,3]-dioxolan-4-yl)-methylamine, illustrating the importance and wide applicability of this compound(82954-65-2).

Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics