107864-73-3

Upstream product

• 108-67-8 1,3,5-trimethyl-benzene 
• 21988-87-4 1,3,5-tris(bromomethyl)-2,4,6-trimethylbenzene 

Downstream Products

• 1243247-20-2 C₅₇H₅₄N₁₂ 
• 1529763-54-9 C₁₈H₂₇N₂₁ 
• 1332499-60-1 C₅₁H₉₃N₁₅O₁₂Si₃ 
• 1239585-60-4 C₆(CH₃)3(CH₂PN₃CC(CH₃)3)3 
• 1239585-61-5 C₁₈H₂₄N₉P₃ 
• 1256839-09-4 C₅₁H₅₁N₉O₁₅ 
• 1260113-62-9 C₂₇H₄₈N₆ 
• 1260113-60-7 C₂₇H₄₂N₆O₃ 
• 1196532-66-7 C₆₆H₅₇N₉O₆ 
• 149525-64-4 1,3,5-tris(aminomethyl)-2,4,6-trimethylbenzene 

Relevant academic research and scientific papers

Design and synthesis of cage-like NADH model molecule intermediate with multi-chiral centers

Studying NADH molecules is one of the most active areas in biomimetic research. It is important to design novel and efficient chiral NADH model molecules. Herein, a cage-like NADH model with multi-chiral centers was designed, and key intermediates have been synthesized. In this study, we found that pentafluorophenoxy group is an excellent leaving group for our synthetic route.

A bright entry to improve the performance of DSSCs with the influence of novel optoelectronic acridinedione based macromolecules in I-/I 3- electrolytes

The performance of Ru(ii) dye-sensitized nanocrystalline TiO2 solar cells (DSSCs) is described with newly synthesized multivalent macromolecules, containing excellent optoelectronic acridinedione linked with 1,2,3-triazole units, via a novel and convenient Cu(I)-catalyzed alkyne and azide 1,3-dipolar cycloaddition (CuAAC) reaction. These unique macromolecules have proved to be highly suitable for utilizing additives in I -/I3- redox couple electrolytes. Among the various substitutions, the maximum photo-current conversion efficiency of about 6.4% with a Voc of 810 mV was obtained with electron rich substitutions in the nitrogen heteroatom.

Topological correspondence between crystal structure of 2,4,6-trimethylbenzene-1,3,5-tris(methanaminium) 2,4,6-trimethylbenzene-1,3,5-triacetate and cesium chloride

Solid-state self-assembly of 2,4,6-trimethylbenzene-1,3,5-tris(methanaminium) 2,4,6-trimethylbenzene-1,3,5-triacetate is mediated by hydrogen bonding. It gives rise to three-dimensional network of hydrogen bonds in which each trication is coordinated with

Synthesis and anticancer activity of bile acid dendrimers with triazole as bridging unit through click chemistry

Triazole-based novel dendrimers with bile acid surface groups have been synthesized through click chemistry by divergent approach and characterized by spectral data. All the dendrimers exhibit excellent anticancer activity. Higher-generation dendrimers exhibit better anticancer activity than the lower-generation dendrimers.

A cascade Aza-Cope/Aza-prins cyclization leading to piperidine derivatives

The cascade aza-Cope/aza-Prins cyclization of homoallylamines to give substituted piperidines has been explored. The use of glyoxalic acid as the carbonyl component afforded bicyclic structures as a result of the internal carboxylate anion trapping the intermediate cation. The unimolecular bis-, tris-, and tetrakis(homoallylamine)s efficiently delivered the appended bis-, tris- and tetrakis(piperidine-4-ol)s (tripod and crucifix shape, respectively) as new entities. The latter compound served as an excellent ligand in the Suzuki-Miyaura cross-coupling reaction to synthesize incrustoporin. The cascade aza-Cope/aza-Prins cyclization of homoallylamines to give substituted piperidines is described. A unimolecular tetrapiperidine derivative, which resulted from this strategy, was employed as a ligand in the Suzuki-Miyaura cross-coupling reaction of an α-iodobutenolide with an arylboronic acid in an efficient synthesis of incrustoporin and its analogues.

Synthesis, anti-microbial activity and molecular docking studies on triazolylcoumarin derivatives

A series of triazolylcoumarins was synthesized by the cycloaddition of acetylenic derivatives to azide in the presence of Cu(I) catalyst at room temperature. All the synthesized compounds were evaluated for their anti-microbial activity against Gram-posit

A chemosensor built with rhodamine derivatives appended to an aromatic platform via 1,2,3-triazoles: Dual detection of aluminum(III) and fluoride/acetate ions

A triazole-ring-appended rhodamine dye (L) has been synthesized that serves as a chromogenic and fluorogenic sensor for dual sensing of aluminum(III) and fluoride or acetate ions specifically.

Simpler and more efficient strategy to stabilize the chromophore orientation in electro-optic polymers with copper-free thermal Huisgen reaction

A new strategy is proposed to stabilize the electro-optic (EO) activity of second-order materials using copper-free thermal Huisgen 1,3-dipolar cross-linking reaction. It consists in freezing the chromophores orientation after the poling process by a cross-linking reaction based on the 1,3-dipolar cycloaddition between an azide and an alkyne. To reach this goal, the synthesis of new methacrylate type polymers bearing a derivative of Disperse Red 1 chromophore was performed. The polymeric structure is bearing a cross-linkable function on its backbone and the complementary reactive function is brought by a small molecule called "doping agent" (DA), containing several complementary cross-linking groups, evenly distributed in the polymer film. Materials have been prepared and exhibit large second-order nonlinear optical coefficients (d33) up to 60 pm/V at the fundamental wavelength of 1064 nm. Moreover, the thermal stability of the orientation of the chromophores could reach 150 °C upon cross-linking with such materials, which is higher than previously described cross-linkable EO polymers based on this reaction. Furthermore, this new strategy widens the possibilities offered by copper-free thermal Huisgen 1,3-dipolar cycloaddition as cross-linking reaction for EO polymers.

C3-symmetric proline-functionalized organocatalysts: Enantioselective michael addition reactions

C3-Symmetric, tripodal catalyst 4 based on 1,3,5- triethylbenzene, which incorporates the features of a molecular receptor, is shown to catalyze Michael addition reactions ofcarbonyl compounds to β-nitrostyrenes in a high stereoselectivity (up to 99:1a dr and up to 98%ee). Copyright

Benzene-based tripodal isothiouronium compounds as sulfate ion receptors

Novel benzene-based tripodal isothiouronium receptors are synthesized for the selective recognition of tetrahedral oxoanions. The binding study by isothermal titration calorimetry indicates that the cationic receptors bind sulfate ions preferably in a tripodal mode, while they show a mixed binding mode toward phosphate ion. The tripodal isothiouronium receptors show large ΔG0 values toward sulfate ions in methanol, which are entropy driven. The results demonstrate that a subtle structural constraint can lead to different binding modes toward structurally similar anions.