TCI R0124 192139-90-5 RuCl[(S,S)-Tsdpen](p-cymene) is a chiral catalyst used in asymmetric synthesis to facilitate stereoselective reactions. This compound plays a crucial role in organic chemistry laboratories where precise control over the stereochemistry of products is essential. Its unique structure allows it to act as a highly efficient chiral catalyst, guiding chemical reactions toward the desired enantiomer with high specificity. This makes it an indispensable tool for researchers aiming to produce optically active compounds with controlled stereochemistry.
The compound is known for its high reactivity and stability, which contribute to its effectiveness in catalytic processes. Its chiral nature enables it to selectively interact with substrates, promoting the formation of specific stereoisomers. This selectivity is vital in applications such as pharmaceutical development, where the stereochemistry of a compound can significantly affect its biological activity. Its ability to maintain activity without significant degradation further enhances its reliability in laboratory settings.
In Indonesian laboratories, this compound is widely used in organic chemistry research, particularly in asymmetric synthesis and the development of new compounds. It is a preferred choice for institutions and research centers that require precise control over stereochemical outcomes. Its application extends to the pharmaceutical and chemical industries, where it supports the creation of bioactive compounds and advanced chemical products.
TCI brochures (PDF)
- Ruthenium Complex Catalysts for Asymmetric Transfer Hydrogenation of Ketons 2026-01-30 · p. 2
- Hydrogenation Catalysts 2025-11-10 · p. 7
Related TCI products
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- TCI R0159 944451-33-6 [RuCl(p-cymene)((S)-dtbm-segphos(regR))]Cl
- TCI R0155 944451-29-0 [RuCl(p-cymene)((S)-segphos(regR))]Cl
- TCI R0154 944451-28-9 [RuCl(p-cymene)((R)-segphos(regR))]Cl
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- Asymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral structure, which enables precise control over the stereochemistry of reaction products.
- Pharmaceutical Research: It is used in drug development to produce optically active compounds with specific stereochemical configurations.
- Organic Chemistry Studies: It supports research in organic chemistry by facilitating stereoselective reactions in laboratory settings.
- Catalytic Processes: Its high reactivity and stability make it suitable for catalytic applications requiring efficient and selective reactions.
- Bioactive Compound Development: It is employed in the synthesis of bioactive compounds, where stereochemistry plays a critical role in biological activity.
| Brand | TCI |
|---|---|
| CAS number | 192139-90-5 |
| 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 or powder, depending on the packaging |
| 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 keep it in a sealed container to prevent exposure to moisture and air, which could affect its performance. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid direct contact with skin or inhalation of vapors. It is important to store it in a well-ventilated area and ensure that it is not exposed to extreme temperatures. Regular inspection of storage conditions is advised to maintain the integrity of the compound throughout its shelf life.
References cited in the TCI brochure
- Akio Fujii. Ruthenium(II)-Catalyzed Asymmetric Transfer Hydrogenation of Ketones Using a Formic Acid−Triethylamine Mixture Journal of the American Chemical Society, 1996. doi:10.1021/ja954126l
- Kazuhiko Matsumura. Asymmetric Transfer Hydrogenation of α, β-Acetylenic Ketones Journal of the American Chemical Society, 1997. doi:10.1021/ja971570a
- Nobuyuki Uematsu. Asymmetric Transfer Hydrogenation of Imines Journal of the American Chemical Society, 1996. doi:10.1021/ja960364k
Product Categories
- Asymmetric SynthesisChiral Catalysts, Chiral Ligands, Chiral ReagentsHydrogenation [Asymmetric Synthesis]
- Catalysis and Inorganic ChemistryHydrogenation [Catalysis]Asymmetric Hydrogenation Catalysts
- Catalysis and Inorganic ChemistryTransition Elements [Catalysis and Inorganic Chemistry]Ruthenium [Catalysis and Inorganic Chemistry]
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