(4R,5R)-(-)-2,2-Dimethyl-α,α,α',α'-tetraphenyl-1,3-dioxolane-4,5-dimethanol, (R,R)-TADDOL

Catsyn offer gram to tons of (4R,5R)-(-)-2,2-Dimethyl-α,α,α',α'-tetraphenyl-1,3-dioxolane-4,5-dimethanol, (R,R)-TADDOL | CAS 93379-48-7, its formula is C31H30O4, molecular weight is 466.574g/mol and the purity is usually 98% Min..

Synonyms : ((4R,5R)-2,2-DIMETHYL-1,3-DIOXOLANE-4,5-DIYL)BIS(DIPHENYLMETHANOL);(-)-(4R,5R)-2,2-DIMETHYL-ALPHA,ALPHA,ALPHA',ALPHA'-TETRAPHENYL-1,3-DIOXOLANE-4,5-DIMETHANOL;(-)-2,3-O-ISOPROPYLIDENE-1,1,4,4-TETRAPHENYL-L-THREITOL;(-)-2,3-O-ISOPROPYLIDENE-1,1,4,4-TETRPHENYL-L-THREITOL;(-)-4,5-BIS[HYDROXY(DIPHENYL)METHYL]-2,2-DIMETHYL-1,3-DIOXOLANE;(-)-TADDOL;(-)-TRANS-4,5-BIS-(DIPHENYL-HYDROXYMETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE;(-)-TRANS-ALPHA,ALPHA'-(2,2-DIMETHYL-1,3-DIOXANE-4,5-DIYL)BIS(DIPHENYLMETHANOL);(-)-TRANS-ALPHA,ALPHA'-(2,2-DIMETHYL-1,3-DIOXOLANE-4,5-DIYL)BIS(DIPHENYLMETHANOL);(-)-TRANS-ALPHA,ALPHA'-(DIMETHYL-1,3-DIOXOLANE-4,5-DIYL)BIS(DIPHENYLMETHANOL);(2R,3R)-(-)-1,1,4,4-TETRAPHENYL-2,3-(2-PROPYLIDENEDIOXY)-BUTANE-1,4-DIOL;(2R,3R)-(-)-4,5-BIS(DIPHENYLHYDROXYMETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE;(2R,3R)-2,3-O-ISOPROPYLIDENE-1,1,4,4-TETRAPHENYL-1,2,3,4-BUTANETETROL;(4R,5R)-(-)-2,2-DIMETHYL-ALPHA,ALPHA,ALPHA',ALPHA'-TETRAPHENYL-1,3-DIOXOLANE-4,5-DIMETHANOL;(4R,5R)-2,2-DIMETHYL-A,A,A',A'-TETRAPHENYLDIOXOLANE-4,5-DIMETHANOL;(4R,5R)-2,2-DIMETHYL-ALPHA,ALPHA,ALPHA',ALPHA'-TETRAPHENYLDIOXOLANE-4,5-DIMETHANOL;(4R,5R)-4,5-BIS(DIPHENYLHYDROXYMETHYL)-2,2-DIMETHYLDIOXOLANE;(R,R)-TADDOL;1,1,4,4-TETRAPHENYL-2,3-O-ISOPROPYLIDENE-L-THREITOL;2,3-O-ISOPROPYLIDENE-1,1,4,4-TETRAPHENYL-L-THREITOL;ALPHA'-TETRAPHENYLDIOXOLANE-4,5-DIMETHANOL;SEEBACH REAGENT;TADDOL;[(4R,5R)-5-(HYDROXY-DIPHENYL-METHYL)-2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL]-DIPHENYL-METHANOL;(4R,5R)-(-)-2,2-Dimethyl-α,α,α',α'-tetraphenyl-1,3-dioxolane-4,5-dimethanol, (R,R)-TADDOL

This substance (CAS No.: 93379-48-7), used as a catalyst and ligand, typically contains specific functional groups or metal binding sites in its molecular structure, endowing it with unique physicochemical properties. Its electronic effects can be modulated by the electron-withdrawing or electron-donating characteristics of substituents, affecting the intramolecular charge distribution and thus regulating the energy level structure and conjugated system range. The expansion of the conjugated system can enhance molecular orbital overlap, improve stability, and lower the activation energy of the reaction, thereby optimizing catalytic activity. Regarding coordination performance, this substance may form stable coordination bonds with the metal center through lone pairs of electrons or π electrons. Its coordination geometry (e.g., tetrahedral, octahedral) and coordination field strength directly affect the redox capacity and intermediate stability in the catalytic cycle. Furthermore, its thermodynamic stability and chemical inertness allow it to maintain structural integrity even under harsh reaction conditions, while its kinetic flexibility supports rapid coordination-dissociation processes, ensuring highly efficient catalytic conversion. In application areas, this substance can be widely used as a catalyst in organic synthesis reactions, such as asymmetric catalysis, cross-coupling reactions, or redox processes. It significantly improves yield and selectivity by lowering the reaction energy barrier and reduces byproduct formation. As a ligand, it can form complexes with transition metals (such as palladium, ruthenium, and iridium) for photocatalysis, electrocatalysis, or homogeneous catalysis systems, playing a crucial role in energy conversion (such as water splitting for hydrogen production and CO₂ reduction) or the synthesis of fine chemicals. In the field of OLED materials, its coordination properties can be used to design emissive or transport layer materials, optimizing device efficiency and lifetime by regulating metal-ligand interactions. Its industry value lies in its high activity and selectivity, which can reduce energy consumption and costs in industrial production. Simultaneously, its structural designability provides a platform for the development of novel catalytic systems, promoting advancements in green chemistry and high-end manufacturing technologies.