(S)-(+)-1,1'-Binaphthol-2,2'-bis(trifluoromethanesulfonate) CAS 128544-05-8: A Key Chiral Reagent for Asymmetric Synthesis and Catalysis
Unlock advanced synthetic pathways with (S)-(+)-1,1'-Binaphthol-2,2'-bis(trifluoromethanesulfonate), a premium chiral reagent from NINGBO INNO PHARMCHEM CO.,LTD. Expertly manufactured in China, we offer high purity solutions for your critical chemical synthesis needs.
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(S)-(+)-1,1'-Binaphthol-2,2'-bis(trifluoromethanesulfonate)
As a trusted supplier in China, NINGBO INNO PHARMCHEM CO.,LTD. presents (S)-(+)-1,1'-Binaphthol-2,2'-bis(trifluoromethanesulfonate), a highly versatile chiral reagent crucial for asymmetric synthesis and catalysis. Its unique structure, featuring a binaphthol backbone functionalized with trifluoromethanesulfonate groups, enhances reactivity and solubility, making it an indispensable tool for chemists aiming to produce enantiomerically pure compounds with high precision. We pride ourselves on being a reliable manufacturer in China, ensuring consistent quality and supply for your research and development needs.
- Leverage our expertise in chiral reagent supply to achieve superior results in enantiomerically pure compound synthesis, a critical aspect of pharmaceutical intermediate manufacturing.
- Discover the power of advanced organic synthesis reagents by incorporating this BINOL derivative into your catalytic processes, driving innovation in fine chemical synthesis tools.
- Trust NINGBO INNO PHARMCHEM CO.,LTD. as your go-to source for high-purity chiral catalysts that enable breakthroughs in enantioselective synthesis strategies.
- Benefit from our commitment to quality as a leading manufacturer in China, providing essential components for cutting-edge asymmetric synthesis research.
Advantages You Gain
Enhanced Stereochemical Control
Utilize this advanced chiral reagent to precisely control stereochemistry in your reactions, leading to higher yields of desired enantiomers. This is fundamental for creating effective pharmaceutical intermediate manufacturing processes.
Improved Reaction Efficiency
The trifluoromethanesulfonate groups boost reactivity and solubility, optimizing reaction conditions and streamlining complex organic synthesis. This makes it a top choice for fine chemical synthesis tools.
Versatile Catalytic Applications
As a key component in chiral catalysts and ligands, it opens doors to novel enantioselective synthesis strategies and advancements in material science.
Key Applications
Asymmetric Synthesis
Employ this compound as a chiral auxiliary to guide the formation of specific stereoisomers, essential for developing drugs with targeted efficacy.
Catalysis
Serve as a precursor for chiral catalysts, enabling highly selective reactions that are vital in modern organic chemistry.
Organic Chemistry Research
A fundamental building block for creating complex molecules and exploring novel reaction pathways, supporting advancements in chiral reagent supply.
Pharmaceutical Development
Crucial for synthesizing enantiomerically pure active pharmaceutical ingredients (APIs), ensuring drug safety and efficacy.