RuCl[(S,S)-Fsdpen](p-cymene) TCI R0122

Chemical Identity

CAS No.: 1026995-72-1
PubChem: CID 91972045·SID 253659539
Formula: C30H28ClF5N2O2RuS
Molecular weight: 712.1 g/mol
Purity: >90%(NMR)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [(1S,2S)-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-NWMPYMMKSA-M

Rp 1.881.600,00

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Berat 200mg 1g

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TCI R0122 1026995-72-1 RuCl[(S,S)-Fsdpen](p-cymene) is a chiral catalyst used in asymmetric synthesis to facilitate chemical reactions that produce asymmetric structures. This compound plays a vital role in modern laboratory settings by enabling the selective formation of specific stereoisomers, which is essential for creating molecules with desired biological activities. In research and development, it is a key reagent for achieving high enantioselectivity, making it indispensable for advanced chemical processes.

One of the main reasons this material is preferred is its high catalytic efficiency and stability under various reaction conditions. It maintains its structural integrity during reactions, ensuring consistent performance without degradation. Its ability to control stereochimical outcomes with precision makes it a favored choice in complex synthetic pathways. Additionally, its compatibility with a wide range of solvents and reaction conditions enhances its versatility in laboratory applications.

In Indonesian laboratories, this compound is widely used in organic chemistry and pharmacology research. It supports the development of bioactive compounds and is essential for drug discovery initiatives. Its application in creating chiral molecules with specific biological functions makes it a critical component in both academic and industrial research settings. The compound’s reliability and effectiveness make it a standard tool in advanced chemical synthesis processes.

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 catalyst is ideal for asymmetric synthesis due to its ability to control stereoselectivity, making it essential for producing chiral compounds with high enantioselectivity.
Organic Chemistry Research: It is frequently used in organic chemistry to facilitate complex reactions that require precise stereochemical control, supporting the synthesis of various functional compounds.
Pharmacological Studies: The compound is valuable in pharmacology for creating bioactive molecules, aiding in the development of new therapeutic agents with specific biological activities.
Catalytic Reaction Optimization: Its stability and efficiency make it suitable for optimizing catalytic reactions, allowing researchers to achieve high yields with minimal catalyst consumption.
Industrial Scale Synthesis: It is used in industrial settings to produce chiral compounds at scale, ensuring consistency and quality in large-scale chemical manufacturing processes.

Brand	TCI
CAS number	1026995-72-1
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 light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent contamination and exposure to air. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Proper ventilation is essential when working with this material to minimize inhalation risks. It should not be stored near incompatible substances to avoid any potential chemical interactions. Regular monitoring of storage conditions ensures the compound remains in optimal condition for use in laboratory applications.

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