Basic information Reaction Safety Supplier Related

(S) QuinoxP(R)

Basic information Reaction Safety Supplier Related

(S) QuinoxP(R) Basic information

Product Name:
(S) QuinoxP(R)
Synonyms:
  • (S) QuinoxP
  • QuinoxP
  • (S,S)-QuinoxP*
  • 2,3-Bis[(S)-(1,1-dimethylethyl)methylphosphino]quinoxaline
  • (S,S)-(+)-2,3-Bis(t-butylmethylphosphino)quinoxaline
  • (S,S)-(+)-2,3-Bis(t-butylMethylphosphino)quinoxaline (S,S)-QuinoxP*
  • (S) QuinoxP(R)
  • (S,S)-2,3-Bis(tert-butylmethylphosphino)quinoxaline
CAS:
1107608-80-9
MF:
C18H28N2P2
MW:
334.38
Product Categories:
  • Chiral Phosphine
Mol File:
1107608-80-9.mol
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(S) QuinoxP(R) Chemical Properties

Melting point:
100-105 °C
alpha 
+54.3° (c 1.0, CHCl3)
Boiling point:
447.6±45.0 °C(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
Powder
pka
-0.54±0.59(Predicted)
color 
orange
optical activity
[α]22/D +55°, c = 1 in chloroform
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36/37/38
Safety Statements 
26
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
HS Code 
2933.99.8290
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(S) QuinoxP(R) Usage And Synthesis

Reaction

  1. Ligand for the rhodium-catalyzed, asymmetric hydrogenation of dehydroamino acid esters and α-enamides.
  2. Ligand for the rhodium-catalyzed, asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds.
  3. Ligand for the rhodium-catalyzed, asymmetric alkylative ring opening reaction
  4. Ligand for the palladium-catalyzed asymmetric allylic alkylation and amination of racemic substrates.
  5. Ligand for the ruthenium-catalyzed asymmetric hydrogenation of ketones.
  6. Ligand for the rhodium-catalyzed, asymmetric hydroacylation of 1,1-disubstituted alkenes with aldehydes.
  7. Ligand for the silver-catalyzed asymmetric nitroso aldol reaction.

Uses

(S,S)-(+)-2,3-Bis(tert-butylmethylphosphino)quinoxaline is a useful reagent for organic synthesis of chiral tetraphenylenes, fused lactones and other useful intermediates.

(S) QuinoxP(R)Supplier

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