(S,S)-I-PR-DUPHOS
(S,S)-I-PR-DUPHOS
  • CAS No.:147253-69-8
Other grades of this product :
(S,S)-I-PR-DUPHOS Basic information
Reaction
Product Name:(S,S)-I-PR-DUPHOS
Synonyms:(S,S)-I-PR-DUPHOS;(-)-1,2-BIS((2S,5S)-2,5-DI-I-PROPYLPHOSPHOLANO)BENZENE;(-)-1,2-BIS((2S,5S)-2,5-DIISOPROPYLPHOSPHOLANO)BENZENE;(-)-1,2-Bis[(2S,5S)-2,5-diisopropylphospholano]benzene, Kanata purity;(-)-1,2-Bis((2S,5S)-2,5-di-i-propylphospholano)benzene,98+%(S,S)-i-Pr-DUPHOS;(-)-1,2-Bis((2S,5S)-2,5-di-i-propylphospholano)benzene (S,S)-i-Pr-DUPHOS;1,2-bis((2S,5S)-2,5-diisopropylphospholan-1-yl)benzene;1,2-Bis[(2S,5S)-2,5-diisopropyl-1-phospholanyl]benzene, 97+%
CAS:147253-69-8
MF:C26H44P2
MW:418.58
EINECS:
Product Categories:organophosphine ligand
Mol File:147253-69-8.mol
(S,S)-I-PR-DUPHOS Chemical Properties
Melting point 40°C
alpha -85° (c 1, hexane)
Boiling point 502.0±20.0 °C(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form crystal
color white
Sensitive Air Sensitive
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
WGK Germany 3
MSDS Information
(S,S)-I-PR-DUPHOS Usage And Synthesis
Reaction
  1. The DUPHOS family of catalysts is highly efficient for the asymmetric hydrogenation of various substituted acetamidoacrylates and enol acetates yielding products of high enantiomeric excesses. Efficient ligand for the asymmetric hydrogenation of tetrasubstituted enamides.
  2. Forms superior catalysts for asymmetric reductive aminations.
  3. Catalyst used for the asymmetric hydrogenation of enol phosphonates.
  4. A novel enantioselective synthesis of β-amino alcohols and 1,2-diamines.
  5. Ligand for the catalytic asymmetric [4+1] cycloaddition of vinylallenes with CO.
  6. Ligand for the Rh-catalyzed asymmetric enyne cycloisomerization.
  7. Catalytic enantioselective addition of dialkylzinc to N-Diphenylphosphinoylimines.
  8. Palladium catalyzed asymmetric phosphination.
  9. Catalytic enantioselective allylation of ketones.
  10. Enantioselective synthesis of cyclopropylborates.
  11. Ligand used in gold catalyzed rearrangement of cyclopropylidene.
(S,S)-I-PR-DUPHOS Preparation Products And Raw materials

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