103883-30-3

Usage

Uses

Used in Scientific Research:
[(4S)-2,2-Dimethyl-1,3-dioxolan-4-yl]methanamine is used as a research compound for studying its chemical properties and potential interactions with other molecules. Its unique structure and properties make it a valuable tool in the exploration of new chemical reactions and processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [(4S)-2,2-Dimethyl-1,3-dioxolan-4-yl]methanamine is used as an intermediate compound in the synthesis of other pharmaceuticals. Its basic and ether-like properties allow it to form stable bonds with various functional groups, making it a versatile building block for the development of new drugs.
Used in Chemical Manufacturing:
[(4S)-2,2-Dimethyl-1,3-dioxolan-4-yl]methanamine is used as a key component in the production of specialty chemicals. Its unique structure and properties enable it to be incorporated into a wide range of chemical products, from solvents to polymers, expanding the possibilities for innovative applications in various industries.

InChI:InChI=1/C6H13NO2/c1-6(2)8-4-5(3-7)9-6/h5H,3-4,7H2,1-2H3/t5-/m1/s1

Upstream product

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Relevant academic research and scientific papers

Stereochemistry-Controlled Supramolecular Architectures of New Tetrahydroxy-Functionalised Amphiphilic Carbocyanine Dyes

The syntheses of novel amphiphilic 5,5′,6,6′-tetrachlorobenzimidacarbocyanine (TBC) dye derivatives with aminopropanediol head groups, which only differ in stereochemistry (chiral enantiomers, meso form and conformer), are reported. For the achiral meso form, a new synthetic route towards asymmetric cyanine dyes was established. All compounds form J aggregates in water, the optical properties of which were characterised by means of spectroscopic methods. The supramolecular structure of the aggregates is investigated by means of cryo-transmission electron microscopy, cryo-electron tomography and AFM, revealing extended sheet-like aggregates for chiral enantiomers and nanotubes for the mesomer, respectively, whereas the conformer forms predominately needle-like crystals. The experiments demonstrate that the aggregation behaviour of compounds can be controlled solely by head group stereochemistry, 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.