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CAS 944450-43-5

RuCl2[(R)-dm-segphos(regR)][(R)-daipen] TCI R0129

RuCl2[(R)-dm-segphos(regR)][(R)-daipen] TCI R0129

Chemical Identity

CAS No.
944450-43-5
PubChem
CID 91972049·SID 253659544
Formula
C65H70Cl2N2O6P2Ru
Molecular weight
1209.2 g/mol
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
[4-[5-bis(3,5-dimethylphenyl)phosphanyl-1,3-benzodioxol-4-yl]-1,3-benzodioxol-5-yl]-bis(3,5-dimethylphenyl)phosphane;(2R)-1,1-bis(4-methoxyphenyl)-3-methylbutane-1,2-diamine;ruthenium(2+);dichloride
SMILES
CC1=CC(=CC(=C1)P(C2=C(C3=C(C=C2)OCO3)C4=C(C=CC5=C4OCO5)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
UDSABKQFPIPYOT-OEGAAENXSA-L
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This compound, TCI R0129 944450-43-5 RuCl2[(R)-dm-segphos(regR)][(R)-daipen], is a complex chiral catalyst used in asymmetric synthesis. It plays a crucial role in laboratories where precise control over reaction outcomes is essential, particularly in reactions requiring enantioselectivity. The compound is designed to facilitate the formation of chiral products with high stereochemical control, making it a valuable tool in synthetic chemistry. Its chiral ligand components are integral in directing chemical reactions toward specific asymmetric structures, enhancing the efficiency of synthesis processes.

The compound's unique properties make it a preferred choice for researchers working in asymmetric catalysis. Its chiral structure enables selective reaction pathways, reducing the need for additional purification steps and increasing overall yield. Additionally, it exhibits stability under controlled laboratory conditions, ensuring consistent performance across multiple experiments. This stability, combined with its ability to catalyze complex reactions, makes it a reliable reagent for advanced synthetic applications.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in asymmetric synthesis and the development of bioactive compounds. Researchers in academic and industrial settings rely on its performance to achieve high-quality results in their experiments. Its application is widespread in pharmaceutical and chemical research, where precise stereochemical control is critical for producing active pharmaceutical ingredients.

  • Asymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral ligand structure, which enables precise enantioselective reactions.
  • Pharmaceutical Research: It is widely used in pharmaceutical research to produce bioactive compounds with specific stereochemistry, essential for drug development.
  • Organic Chemistry Studies: Its role in organic chemistry studies is significant, especially in creating complex molecules with controlled stereochemistry.
  • Chiral Catalyst Development: It is a preferred catalyst in the development of new chiral catalysts, offering high efficiency and selectivity in synthetic reactions.
  • Bioactive Compound Synthesis: Its ability to direct reactions toward specific products makes it valuable in the synthesis of compounds with biological activity.

Brand TCI
CAS number 944450-43-5
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Catalysts, Chiral Ligands, Chiral Reagents
Pack sizes Available in various pack sizes as per supplier specifications
Physical form Solid or powder, depending on the formulation
Storage Store in a cool, dry place away from moisture and light

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 degrade its properties. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid contact with incompatible substances to ensure safety during handling and storage. Regular inspection of storage conditions is advised to ensure optimal performance and safety in laboratory settings.

References cited in the TCI brochure

  1. Cheng-yi Chen. Concise Asymmetric Synthesis of (+)-Conocarpan and Obtusafuran Synlett, 2012. doi:10.1055/s-0032-1317704