(R)-(-)-1,1'-Bi-2-naphthol bis(trifluoromethanesulfonate)

Catsyn offer gram to tons of (R)-(-)-1,1'-Bi-2-naphthol bis(trifluoromethanesulfonate) | CAS 126613-06-7, its formula is C22H12F6O6S2, molecular weight is 550.451g/mol and the purity is usually 98% Min..

Synonyms : (R)-(-)-1,1'-BI-2,2'-NAPHTHOL BIS(TRIFLUOROMETHANESULFONATE);(R)-(-)-1,1'-BI-2-NAPHTHOL BIS(TRIFLUOROMETHANESULFONATE);(R)-(-)-1,1'-BI-2-NAPHTHOL-BIS(TRIFLUOROMETHANESULPHONATE);(R)-(-)-1,1'-BI-2-NAPHTHYL BIS(TRIFLUOROMETHANESULFONATE);(R)-(-)-1,1'-BINAPHTHALENE-2,2'-DIYLBIS(TRIFLUOROMETHANESULFONATE);(R)-(-)-1,1'-BINAPHTHOL-2,2'-BIS(TRIFLUOROMETHANESULFONATE);(R)-(-)-1,1'-BIS(2-NAPHTHOL) DITRIFLATE;(R)-(-)-BINOL-TF2;(R)-1,1'-BI(2-NAPHTHOL) BIS(TRIFLUOROMETHANESULFONATE);(R)-1,1'-BINAPHTHALENE-2,2'-DIYL BIS(TRIFLUOROMETHANESULFONATE);(R)-1,1'-BINAPHTHYL-2,2'-DIYL BIS(TRIFLUOROMETHANE)SULPHONATE;(R)-BINOL-TF2;(R)-TRIFLUOROMETHANESULFONIC ACID 2'-TRIFLUOROMETHANESULFONYLOXY-[1,1']BINAPHTHALENYL-2-YL ESTER;(S)-(+)-1,1'-BI-2,2'-NAPHTHOL BIS(TRIFLUOROMETHANESULFONATE);(S)-(+)-1,1'-BI-2-NAPHTHOL BIS(TRIFLUOROMETHANESULFONATE);(S)-(+)-1,1'-BI-2-NAPHTHOL-BIS(TRIFLUOROMETHANESULPHONATE);(S)-(+)-1,1'-BI-2-NAPHTHYL BIS(TRIFLUOROMETHANESULFONATE);(S)-(+)-1,1'-BINAPHTHALENE-2,2'-DIYLBIS(TRIFLUOROMENTHANESULFONATE);(S)-(+)-1,1'-BINAPHTHOL-2,2'-BIS(TRIFLUOROMETHANESULFONATE);(S)-(+)-1,1'-BIS(2-NAPHTHOL) DITRIFLATE;(S)-(+)-BINOL-TF2;(S)-(-)-1,1'-BI-2-NAPHTHOL BIS(TRIFLUOROMETHANESULFONATE);(S)-1,1'-BI(2-NAPHTHOL) BIS(TRIFLUOROMETHANESULFONATE);(S)-1,1'-BINAPHTHALENE-2,2'-DIYL BIS(TRIFLUOROMETHANESULFONATE);(S)-1,1'-BINAPHTHYL-2,2'-DIYL BIS(TRIFLUOROMETHANESULPHONATE);(S)-BINOL-TF2;(S)-TRIFLUOROMETHANESULFONIC ACID 2'-TRIFLUOROMETHANESULFONYLOXY-[1,1']BINAPHTHALENYL-2-YL ESTER;1,1'-BI-2-NAPHTHOL BIS(TRIFLUOROMETHANESULFONATE);1,1'-BI-2-NAPHTHOL-BIS(TRIFLUOROMETHANESULPHONATE);1,1'-BINAPHTHYL-2,2'-DIYL BIS(TRIFLUOROMETHANE)SULPHONATE;1,1'-BINAPHTHYL-2,2'-DIYL BIS(TRIFLUOROMETHANESULFONATE);1,1'-BIS(2-NAPHTHOL) DITRIFLATE;BINOL-TF2;R)-(-)-1,1'-BINAPHTHYL-2,2'-DIYL BIS(TRIFLUOROMETHANESULFONATE;R-1-(2-[(TRIFLUOROMETHANE)SULFONYLOXY]NAPHTHALEN-1-YL)NAPHTHALEN-2-YL TRIFLUOROMETHANESULFONATE;S)-(+)-1,1'-BINAPHTHYL-2,2'-DIYL BIS(TRIFLUOROMETHANESULFONATE;S-1,1'-BINAPHTHOL-2,2'-BIS(TRIFLUOROMETHANESULFONATE);TRIFLUOROMETHANESULFONIC ACID 2'-TRIFLUOROMETHANESULFONYLOXY-[1,1']BINAPHTHALENYL-2-YL ESTER

This substance (CAS No.: 126613-06-7), acting as both a catalyst and a ligand, typically possesses unique physicochemical properties due to the presence of specific functional groups or metal binding sites in its molecular structure. Its electronic effects can be modulated by the electron-withdrawing or electron-donating properties of substituents, thereby influencing the distribution of molecular orbital energy levels, particularly the energy gaps between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO), which is crucial for electron transfer processes in catalytic reactions. The expansion of the conjugated system enhances intramolecular π-electron delocalization, improves stability, and optimizes coordination geometry, maintaining structural integrity during catalytic cycles. As a catalyst, its active center can promote substrate activation and lower reaction energy barriers by coordinating with unsaturated metal sites or acidic/basic sites; as a ligand, its steric hindrance and electron-donating ability can finely modulate the electronic state and geometry of the metal center, thus affecting catalytic selectivity. Regarding stability, this substance exhibits good solubility and thermal stability in common solvents and maintains catalytic activity over a wide temperature range. In application fields, this substance serves extensively as a catalyst and ligand in organic synthesis, homogeneous catalysis, and materials science. In organic synthesis, it efficiently catalyzes key steps such as cross-coupling reactions and asymmetric hydrogenation, significantly improving reaction yield and enantioselectivity while reducing byproduct formation. In homogeneous catalysis, as a ligand for metal complexes, it can optimize catalytic performance by modulating the electronic environment of the metal center, enabling applications in industrial processes such as olefin polymerization and CO₂ conversion, achieving green chemistry goals. In materials science, this substance can participate as a functional ligand in the construction of metal-organic frameworks (MOFs) or coordination polymers, endowing materials with specific optical, electrical, and magnetic properties, expanding its applications in OLED displays, sensors, and catalytic supports. Its core value lies in achieving precise control of catalytic performance and material function through molecular design, providing key technological support for chemical manufacturing and high-end material development, and driving related industries towards high efficiency and sustainability.