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1107608-80-9

1107608-80-9 Structure

1107608-80-9 Structure
IdentificationBack Directory
[Name]

(S) QuinoxP(R)
[CAS]

1107608-80-9
[Synonyms]

QuinoxP
(S) QuinoxP
(S,S)-QuinoxP*
(S) QuinoxP(R)
3-bis((S)-tert-butyl(methyl)phosphino)quinoxaline
(S,S)-2,3-Bis(tert-butylmethylphosphino)quinoxaline
(S,S)-(+)-2,3-Bis(t-butylmethylphosphino)quinoxaline
2,3-Bis[(S)-(1,1-dimethylethyl)methylphosphino]quinoxaline
[Molecular Formula]

C18H28N2P2
[MDL Number]

MFCD10567042
[MOL File]

1107608-80-9.mol
[Molecular Weight]

334.38
Chemical PropertiesBack Directory
[Melting point ]

100-105 °C
[alpha ]

+54.3° (c 1.0, CHCl3)
[Boiling point ]

447.6±45.0 °C(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

Powder
[pka]

-0.54±0.59(Predicted)
[color ]

orange
[Optical Rotation]

[α]22/D +55°, c = 1 in chloroform
[InChI]

InChI=1/C18H28N2P2/c1-17(2,3)21(7)15-16(22(8)18(4,5)6)20-14-12-10-9-11-13(14)19-15/h9-12H,1-8H3/t21-,22-/s3
[InChIKey]

DRZBLHZZDMCPGX-ALHZVVSGNA-N
[SMILES]

[P@](C1=NC2C=CC=CC=2N=C1[P@@](C)C(C)(C)C)(C)C(C)(C)C |&1:0,11,r|
Safety DataBack Directory
[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
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Aquatic Chronic 4
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Questions And AnswerBack Directory
[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.
Reactions of 1107608-80-9_1
Reactions of 1107608-80-9_2
Hazard InformationBack Directory
[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.
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