RuCl[(R,R)-Fsdpen](p-cymene) TCI R0123

Chemical Identity

CAS No.: 1026995-71-0
PubChem: CID 71463829·SID 253659540
Formula: C30H28ClF5N2O2RuS
Molecular weight: 712.1 g/mol
Purity: >90%(NMR)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [(1R,2R)-2-amino-1,2-diphenylethyl]-(2,3,4,5,6-pentafluorophenyl)sulfonylazanide;1-methyl-4-propan-2-ylbenzene;ruthenium(2+);chloride
SMILES: CC1=CC=C(C=C1)C(C)C.C1=CC=C(C=C1)[C@H]([C@@H](C2=CC=CC=C2)[N-]S(=O)(=O)C3=C(C(=C(C(=C3F)F)F)F)F)N.[Cl-].[Ru+2]
InChIKey: UWFMZLATRGEOIW-ZJPTYAPPSA-M

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Berat 200mg 1g

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TCI R0123 1026995-71-0 RuCl[(R,R)-Fsdpen](p-cymene) is a chiral catalyst used in asymmetric synthesis, playing a crucial role in laboratories that require precise control over stereochemistry. This compound is specifically designed to facilitate reactions that produce enantiomerically pure products, making it an essential tool in advanced chemical research. Its application spans across various fields, including pharmaceutical and organic chemistry, where the ability to control molecular structure is vital.

The compound's effectiveness stems from its chiral structure, which allows for high selectivity in catalytic processes. It is known for its stability and ability to accelerate chemical reactions without significant degradation, making it a reliable choice for researchers. The unique combination of the (R,R)-Fsdpen ligand and the p-cymene group enhances its catalytic efficiency, enabling it to perform under a wide range of reaction conditions. This makes it a preferred option for laboratories seeking precision and consistency in their synthetic processes.

In Indonesian laboratories, this compound is widely used in scientific research, particularly in organic chemistry and pharmacology. It is a key component in the development of new compounds with high biological activity. Institutions and universities in Indonesia rely on this material for its ability to produce structurally specific products, supporting advancements in drug discovery and chemical synthesis. Its presence in research facilities highlights its importance in modern scientific inquiry.

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

Asymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral nature, enabling the production of enantiomerically pure compounds with high selectivity.
Pharmaceutical Research: It is extensively used in drug development to create molecules with specific stereochemistry, which is crucial for pharmaceutical efficacy and safety.
Organic Chemistry Studies: The compound supports complex organic reactions, allowing researchers to explore new synthetic pathways and molecular structures.
Chiral Catalyst Development: Its stability and catalytic efficiency make it a preferred choice for developing new chiral catalysts in industrial and academic settings.
Biomedical Applications: It plays a role in the synthesis of bioactive compounds, supporting research in areas such as enzyme inhibition and receptor binding.

Brand	TCI
CAS number	1026995-71-0
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 batch
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 affect its performance. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper ventilation in the workspace. Keep the material away from incompatible substances to prevent any potential chemical reactions. Regularly inspect storage conditions to ensure optimal preservation of the compound's properties.

References cited in the TCI brochure

John Limanto. Dynamic Kinetic Resolution: Asymmetric Transfer Hydrogenation of α-Alkyl-Substituted β-Ketoamides Organic Letters, 2009. doi:10.1021/ol902715d