(S)-(+)-1,1'-Binaphthyl-2,2'-diyl Bis(trifluoromethanesulfonate) is a chiral compound widely used in asymmetric synthesis within laboratory settings. This reagent plays a crucial role in catalyzing organic reactions that require precise control over stereochemistry. Its unique structure enables it to act as a chiral catalyst, guiding the formation of specific enantiomers in chemical reactions. This makes it an essential tool for researchers aiming to achieve high selectivity and yield in complex organic transformations.
The compound's chiral nature and high reactivity make it a preferred choice for synthetic chemists. Its ability to selectively influence reaction pathways enhances the efficiency of asymmetric processes. Additionally, its stability under various reaction conditions ensures consistent performance, reducing the need for frequent recalibration or replacement. These properties make it a reliable and effective reagent in both academic and industrial research environments.
In Indonesian laboratories, this compound is extensively used in organic chemistry research, particularly in asymmetric synthesis and the development of new compounds. Its application is critical for producing molecules with specific stereochemical configurations, which are essential in pharmaceutical and materials science research. The compound's versatility and effectiveness have made it a standard component in many chemical laboratories across Indonesia.
TCI brochures (PDF)
- Asymmetric Synthesis 2026-03-18 · p. 3
Related TCI products
- TCI B2230 126613-06-7 (R)-(-)-1,1'-Binaphthyl-2,2'-diyl Bis(trifluoromethanesulfonate)
- TCI B3202 173831-50-0 (R)-2,2'-Bis(methoxymethoxy)-1,1'-binaphthyl
- TCI D4883 211560-97-3 (S)-6,6'-Dibromo-2,2'-bis(methoxymethoxy)-1,1'-binaphthyl
- TCI D4882 179866-74-1 (R)-6,6'-Dibromo-2,2'-bis(methoxymethoxy)-1,1'-binaphthyl
- TCI D3208 18531-95-8 (S)-(-)-1,1'-Binaphthyl-2,2'-diamine
- TCI D3207 18741-85-0 (R)-(+)-1,1'-Binaphthyl-2,2'-diamine
- Asymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral structure, enabling the selective formation of enantiomers with high efficiency.
- Pharmaceutical Research: It is used in drug development to create chiral compounds with specific stereochemistry, which are essential for pharmaceutical applications.
- Organic Chemistry Education: It is commonly used in teaching laboratories to demonstrate the principles of asymmetric catalysis and stereochemical control.
- Catalyst Development: Its reactivity and selectivity make it a valuable tool for developing new chiral catalysts and ligands.
- Industrial Chemical Production: It is applied in industrial settings to produce chiral compounds with high purity and controlled stereochemistry.
| Brand | TCI |
|---|---|
| CAS number | 128544-05-8 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Catalysts, Chiral Ligands, Chiral Reagents |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
This compound should be stored in a cool, dry environment to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to moisture and air, which could degrade its properties. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to minimize any potential risks associated with its chemical composition. Regular inspection of storage conditions is advised to maintain optimal performance and safety in the laboratory setting.
—








