RuCl2[(S)-xylbinap][(S)-daipen] TCI R0132

Chemical Identity

CAS No.: 220114-01-2
PubChem: CID 91972077·SID 253659926
Formula: C71H74Cl2N2O2P2Ru
Molecular weight: 1221.3 g/mol

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [1-[2-bis(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane;(2S)-1,1-bis(4-methoxyphenyl)-3-methylbutane-1,2-diamine;ruthenium(2+);dichloride
SMILES: CC1=CC(=CC(=C1)P(C2=C(C3=CC=CC=C3C=C2)C4=C(C=CC5=CC=CC=C54)P(C6=CC(=CC(=C6)C)C)C7=CC(=CC(=C7)C)C)C8=CC(=CC(=C8)C)C)C.CC(C)[C@@H](C(C1=CC=C(C=C1)OC)(C2=CC=C(C=C2)OC)N)N.[Cl-].[Cl-].[Ru+2]
InChIKey: UTQCNMRDWASSEC-OGLOXHGMSA-L

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Berat 200mg 1g

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TCI R0132 220114-01-2 RuCl2[(S)-xylbinap][(S)-daipen] is a chiral compound designed for use in asymmetric synthesis, playing a critical role in modern chemical laboratories. This material is specifically engineered to facilitate selective chemical reactions, enabling the production of compounds with precise stereochemical configurations. Its application is essential in the development of pharmaceuticals and other complex molecules that require high structural specificity. As a chiral catalyst, it offers a reliable and efficient method for achieving desired chemical outcomes in controlled environments.

One of the key properties that make this compound a preferred choice is its ability to enhance reaction efficiency while maintaining stereochemical control. Its chiral structure ensures that only the desired enantiomer is produced, reducing the need for additional purification steps. Additionally, its stability and effectiveness in various reaction conditions make it a versatile tool for researchers. The compound’s high selectivity and consistent performance contribute to its widespread use in both academic and industrial research settings.

In Indonesian laboratories, this compound is commonly used in scientific research and pharmaceutical development. It supports the creation of high-purity compounds with specific biological activities, which are essential for drug discovery and development. Its availability in practical packaging and solid form makes it suitable for use in a wide range of experimental scales, from small-scale research to larger production processes. Its reliability and performance make it a valuable asset in the chemical research community.

TCI brochures (PDF)

Ruthenium Complex Catalysts for Asymmetric Hydrogenation of Ketons 2024-12-16 · p. 2
Hydrogenation Catalysts 2025-11-10 · p. 8

Related TCI products

Asymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its ability to selectively catalyze reactions, producing enantiomerically pure compounds with high efficiency.
Pharmaceutical Research: It is widely used in pharmaceutical research to develop compounds with specific biological activities, ensuring accurate stereochemical outcomes.
Organic Chemistry Experiments: Its chiral properties make it a preferred choice for organic chemistry experiments requiring precise stereochemical control.
Drug Development: It supports the development of new drugs by enabling the synthesis of compounds with desired stereochemistry and biological activity.
Academic Research: It is a valuable tool for academic research, allowing scientists to explore new chemical reactions and synthetic pathways with high precision.

Brand	TCI
CAS number	220114-01-2
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Catalysts, Chiral Ligands, Chiral Reagents
Pack sizes	Available in various pack sizes for laboratory use
Physical form	Solid
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 maintain its chemical integrity. Due to its chiral nature, it is important to handle it with care to avoid contamination or degradation. Proper labeling and storage conditions are essential to ensure its effectiveness in laboratory applications. Always follow standard laboratory safety protocols when handling this material to maintain a safe working environment.

References cited in the TCI brochure

Takeshi Ohkuma. Asymmetric Hydrogenation of Alkenyl, Cyclopropyl, and Aryl Ketones. RuCl2(xylbinap)(1,2-diamine) as a Precatalyst Exhibiting a Wide Scope Journal of the American Chemical Society, 1998. doi:10.1021/ja983257u
Takeshi Ohkuma. Selective Hydrogenation of Benzophenones to Benzhydrols. Asymmetric Synthesis of Unsymmetrical Diarylmethanols Organic Letters, 2000. doi:10.1021/ol9904139