RuCl[(S,S)-Tsdpen](mesitylene) TCI R0126

Chemical Identity

CAS No.: 174813-81-1
PubChem: CID 25000063·SID 253659919
Formula: C30H33ClN2O2RuS
Molecular weight: 622.2 g/mol
Purity: >90%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [(1S,2S)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;ruthenium(2+);1,3,5-trimethylbenzene;chloride
SMILES: CC1=CC=C(C=C1)S(=O)(=O)[N-][C@@H](C2=CC=CC=C2)[C@H](C3=CC=CC=C3)N.CC1=CC(=CC(=C1)C)C.[Cl-].[Ru+2]
InChIKey: XBNBOGZUDCYNOJ-XCPIVNJJSA-M

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Berat 200mg 1g

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TCI R0126 174813-81-1 RuCl[(S,S)-Tsdpen](mesitylene) is a metal-based complex compound used in asymmetric synthesis. This material serves as a chiral catalyst, enabling the production of chemically specific asymmetric structures. In the laboratory, it plays a crucial role in facilitating chemical reactions that require precise control over the stereochemistry of the final product. Its application is particularly relevant in organic chemistry and pharmaceutical research, where the ability to produce enantiomerically pure compounds is essential.

The compound is known for its stability under certain conditions and its solubility in organic solvents. These properties make it a preferred choice for researchers aiming to achieve high enantiomeric excess in their reactions. It maintains its catalytic activity without significant degradation, ensuring reliable results in repeated experiments. Its effectiveness and consistency contribute to its popularity among scientists working in advanced chemical synthesis.

In Indonesian laboratories, this compound is widely used in organic chemistry research, especially in asymmetric synthesis and drug development. Its ability to produce specific molecular structures makes it a key component in the development of new pharmaceutical compounds. It is a favored material for researchers seeking precision and efficiency in their chemical 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 compound is ideal for asymmetric synthesis due to its chiral catalytic properties, enabling the selective formation of enantiomerically pure products.
Pharmaceutical Research: It is used in drug development to produce compounds with specific stereochemistry, which is critical for drug efficacy and safety.
Organic Chemistry Experiments: Its solubility in organic solvents and stability make it suitable for a wide range of organic reactions requiring precise stereochemical control.
Catalytic Reactions: The compound's ability to maintain catalytic activity without degradation ensures consistent results in repeated chemical processes.
Advanced Chemical Synthesis: It is a preferred choice for complex chemical syntheses where high enantiomeric excess is required for the final product.

Brand	TCI
CAS number	174813-81-1
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Catalysts, Chiral Ligands, Chiral Reagents
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from light

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Storage conditions should ensure that the compound remains stable and retains its catalytic properties. Proper labeling and secure storage are essential to maintain safety in the laboratory environment. Always follow standard chemical handling procedures to minimize risks associated with its use.

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
Issaku Yamada. Asymmetric Transfer Hydrogenation of Benzaldehydes Organic Letters, 2000. doi:10.1021/ol0002119