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TCI

CAS 944450-44-6

RuCl2[(S)-dm-segphos(regR)][(S)-daipen] TCI R0128

RuCl2[(S)-dm-segphos(regR)][(S)-daipen] TCI R0128

Chemical Identity

CAS No.
944450-44-6
PubChem
CID 91972046·SID 253659541
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;(2S)-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-OGLOXHGMSA-L
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TCI R0128 944450-44-6 RuCl2[(S)-dm-segphos(regR)][(S)-daipen] is a chiral ruthenium-based complex used in asymmetric synthesis. This compound serves as a highly effective chiral catalyst in chemical reactions requiring precise stereochemical control. Its chiral nature enables the production of compounds with specific spatial structures, which is crucial in the synthesis of pharmacological and biological compounds. The compound plays a vital role in modern synthetic chemistry by facilitating the creation of enantiomerically pure products.

The compound's key properties include its ability to lower activation energy and enhance reaction efficiency, leading to high enantiomeric excess. Its complex structure, composed of chiral ligands and a ruthenium ion, allows for specific interactions with substrates, improving both the efficiency and selectivity of reactions. This makes it a preferred choice for researchers aiming to achieve high stereocontrol in their synthetic processes.

In Indonesian laboratories, this compound is widely used in organic chemistry research, particularly in asymmetric synthesis and drug development. Due to its specialized nature and limited availability, it is a primary choice for researchers needing precise chiral catalytic systems. Its application is essential in projects requiring high stereochemical control and selectivity.

  • Asymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral structure and ability to control stereochemistry, making it suitable for producing enantiomerically pure compounds.
  • Drug Development: It is used in the development of pharmaceutical compounds where precise stereochemistry is critical for biological activity and efficacy.
  • Organic Chemistry Research: Researchers use it to explore new synthetic pathways and improve reaction efficiency in complex organic transformations.
  • Chiral Catalyst Studies: Its unique structure makes it a valuable tool for studying the behavior and performance of chiral catalysts in various reaction conditions.
  • Biologically Active Compound Synthesis: It enables the synthesis of biologically active compounds with specific spatial configurations, enhancing their pharmaceutical potential.

Brand TCI
CAS number 944450-44-6
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 light to maintain its stability and effectiveness. 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, to ensure laboratory safety. Proper ventilation is essential when working with this material to minimize exposure. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.

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