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ChemicalBook--->CAS DataBase List--->850253-53-1

850253-53-1

850253-53-1 Structure

850253-53-1 Structure
IdentificationBack Directory
[Name]

(R)-(+)-5,5'-Bis[di(3,5-xylyl)phosphino]-4,4'-bi-1,3-benzodioxole,min.98%(R)-DM-SEGPHOS
[CAS]

850253-53-1
[Synonyms]

(R)-DM-SEGPHOS
(R)-DM-SEGPHOS(R)
(R)-(+)-DM-SEGPHOS(regR)
(R)-(+)-DM-SEGPHOS®
(R)-(+)-5,5'-Bis[di(3,5-xylyl)phosphino]-4,4'-bi-1,3-benzodioxole
(R)-(+)-5,5'-Bis[di(3,5-xylyl)phosphino]-4,4'-bi-1,3-benzodioxole,min.98%(R)-DM-SEGPHOS
1,1'-[(4R)-[4,4'-Bi-1,3-benzodioxole]-5,5'-diyl]bis[1,1-bis(3,5-dimethylphenyl)phosphine]
(R)-(+)-5,5'-Bis[di(3,5-xylyl)phosphino]-4,4'-bi-1,3-benzodioxole, min. 98% (R)-(+)-DM-SEGPHOS(R)
[(4R)-(4,4μ-bi-1,3-benzodioxole)-5,5μ-diyl]bis[bis(3,5-dimethylphenyl)phosphine], (R)-(+)-5,5μ-Β:is[di(3,5-xylyl)phosphino]-4,4μ-bi-1,3-benzodioxole
[Molecular Formula]

C46H44O4P2
[MDL Number]

MFCD09753008
[MOL File]

850253-53-1.mol
[Molecular Weight]

722.8
Chemical PropertiesBack Directory
[Melting point ]

256-261 °C
[Boiling point ]

816.9±65.0 °C(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

Powder
[color ]

off white to pale yellow
[optical activity]

[α]20/D +60, c = 0.1 in chloroform
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[WGK Germany ]

3
[HS Code ]

2932.99.7000
Questions And AnswerBack Directory
[Reaction]

  1. Biaryl bisphosphine ligand with narrow dihedral angle. The DM-SEGPHOS ligand, as the ruthenium complex, gives superior enantioselectivity and diastereoselectivity in the asymmetric hydrogenation of α-substituted-β-ketoesters.
  2. Copper catalyzed enantioselective [3 + 2] cycloaddition as a route to γ–amino ketones and 3-pyrrolidinones.
  3. Palladium catalyzed enantioselective addition of malonates to dihydroisoquinolines.
  4. Ruthenium catalyzed enantioselective synthesis of β amino acids by hydrogenation.
  5. Ruthenium catalyzed asymmetric hydrogenation of 3-quinuclidinone. See 44-0098 for Ru catalyst.
  6. Diastereoand enantioselective ruthenium-catalyzed hydrohydroxyalkylation of 2-silyl-butadienes.
  7. Asymmetric [2+2+2] cycloaddition.
  8. Linear selective C-H activation.
Reactions of 850253-53-1_1
Reactions of 850253-53-1_2
Hazard InformationBack Directory
[Uses]

Takasago Ligands and Complexes for Asymmetric Reactions
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