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693200 Sigma-Aldrich

RuCl2[(S)-(DM-SEGPHOS®)][(S,S)-DPEN]

Synonym: Dichloro[(S)-5,5′-bis[di(3,5-xylyl)phosphino]-4,4′-bi-1,3-benzodioxole][(1S,2S)-1,2-diphenylethylenediamine]ruthenium(II)

  • CAS Number 944450-46-8

  • Empirical Formula (Hill Notation) C60H60Cl2N2O4P2Ru

  • Molecular Weight 1107.05

  •  MDL number MFCD09753032

  •  PubChem Substance ID 329761572

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Properties

Related Categories Asymmetric Synthesis, Chemical Synthesis, Chiral Catalysts, Ligands, and Reagents, Privileged Ligands and Complexes, SEGPHOS More...
InChI Key   FOEKPXQPRAIJRW-LISIALKWSA-L
storage temp.   2-8°C

Description

Packaging

50, 100 mg in amber glass bottle

Legal Information

Sold in collaboration with Takasago for research purposes only. JP Registration No. 3148136 JP Appllication No. 19970359654

SEGPHOS is a registered trademark of Takasago Intl. Corp.

Application

Takasago Ligands and Complexes for Asymmetric Reactions

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Takasago Ligands and Complexes for Asymmetric Reactions

The quest to find chiral catalysts capable of achieving high enantiomeric excess for a variety of asymmetric transformations has been an ongoing endeavor for the past 40 years. One of the most releva...
Keywords: Addition reactions, Arylations, Asymmetric synthesis, Catalysis, Hydrogenations, Ligands, transformation

Related Content

Takasago Ligands - Advantages and Applications

Introduction The quest to find chiral catalysts capable of achieving high enantiomeric excess for a variety of asymmetric transformations has been an ongoing endeavor for the past 40 years. One of th...
Keywords: Addition reactions, Applications, Arylations, Asymmetric synthesis, Building blocks, Catalysis, Epoxidations, Hydrogenations, Hydrosilylations, Ligands, Sharpless Epoxidation, transformation

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