23099-64-1

Usage

Uses

Used in Textile Industry:
2,2'-[(6-anilino-1,3,5-triazine-2,4-diyl)diimino]bisethanol is used as a fluorescent whitening agent for enhancing the brightness and whiteness of textiles. Its application in this industry is due to its ability to absorb ultraviolet light and emit visible light, thereby improving the overall appearance of fabrics.
Used in Chemical Production:
In the chemical industry, 2,2'-[(6-anilino-1,3,5-triazine-2,4-diyl)diimino]bisethanol serves as an intermediate in the synthesis of dyes and pigments. Its role in this process is attributed to its chemical structure, which allows for the creation of a wide range of colored compounds.
Used in Pharmaceutical and Medical Research:
2,2'-[(6-anilino-1,3,5-triazine-2,4-diyl)diimino]bisethanol is explored as a potential therapeutic agent for the treatment of various diseases, including cancer and inflammatory conditions. Its application in this field is due to its possible biological activities and interactions with cellular targets, which may contribute to disease management and treatment.

Upstream product

• 54581-55-4 2-chloro-4,6-bis[(2-hydroxyethyl)amino]-1,3,5-triazine 
• 62-53-3 aniline 
• 2272-40-4 2-phenylamino-4,6-dichloro-s-triazine 
• 141-43-5 ethanolamine 

Relevant academic research and scientific papers

Structural investigations of three triazines: Solution-state NMR studies of internal rotation and structural information from solid-state NMR, plus a full structure determination from powder x-ray diffraction in one case

Three model 2,4,6-tris(amino)-1,3,5-triazines, structurally related to a dyestuff molecule previously studied by NMR, were synthesized in order to enable the effects of rotamer exchange on the NMR spectra to be investigated in more detail. Two of the compounds are novel. Internal rotation of the triazine ring substituents was studied by variable-temperature solution-state 1H, 13C and 15N NMR spectroscopy. All the expected rotamers were detected for each molecule. Rotamer exchange rates varied from slow to fast over the temperature range -40 to 90°C, as observed for the dyestuff molecule itself. Solid-state 13C and 15N NMR provided information about the structures of the solid molecules. A full crystal structure determination from high-resolution powder x-ray diffraction was achieved for one of the molecules using simulated annealing techniques. Ab initio MO and 15N NMR chemical shift calculations, based on energy-minimized structures derived from the x-ray structure determination, enabled the effect of intermolecular hydrogen bonding on the 15N NMR chemical shifts to be studied. The results compared favourably with the experimental solid-state 15N NMR shifts. Copyright