| Identification | Back Directory | [Name]
RAC-2-(DI-T-BUTYLPHOSPHINO)-1,1'-BINAPHTHYL | [CAS]
255836-67-0 | [Synonyms]
TrixiePhos
98% TrixiePhos
TrixiePhos 97%
rac-2-(Di-tert-butylphosphino)-1,1
2-(DI-TERT-BUTYLPHOSPHINO)-1,1'-BINAPHTHYL
RAC-2-(DI-T-BUTYLPHOSPHINO)-1,1'-BINAPHTHYL
rac-2-(Di-tert-butylphosphino)-1,1-binaphthyl
2-(Di-tert-butylphosphino)-1,1'-binaphthyl,98%
[1,1'-Binaphthalen]-2-yldi-tert-butylphosphine
RaceMic-2-di-tert-butylphosphino-1,1-binaphthyl
RACEMIC-2-(DI-T-BUTYLPHOSPHINO)-1,1'-BINAPHTHYL
rac-2-(Di-t-butylphosphino)-1,1'-binaphthyl,98%
racemic-2-Di-t-butylphosphino-1,1'-binaphthyl,98%
2-(Di-tert-butylphosphino)-1,1'-binaphthyl ,97.5%
rac-2-(Di-tert-butylphosphino)-1,1'-binaphthyl 97%
raceMic-2-Di-t-butylphosphino-1,1'-binaphthyl TrixiePhos
rac-2-(Di-t-butylphosphino)-1,1'-binaphthyl, (TrixiePhos)
TrixiePhos, [1,1'-binaphthalen]-2-yldi-tert-butylphosphine
PHOSPHINE, [1,1''-BINAPHTHALEN]-2-YLBIS(1,1-DIMETHYLETHYL)-
rac-2-(Di-t-butylphosphino)-1,1'-binaphthyl, 98% (TrixiePhos)
racemic-2-Di-t-butylphosphino-1, 1'-binaphthyl, 98% TrixiePhos | [Molecular Formula]
C28H31P | [MDL Number]
MFCD03094576 | [MOL File]
255836-67-0.mol | [Molecular Weight]
398.52 |
| Chemical Properties | Back Directory | [Appearance]
White to pale yellow crystalline powder | [Melting point ]
148-151 °C
| [Boiling point ]
519.5±29.0 °C(Predicted) | [form ]
crystal | [color ]
white | [InChIKey]
QGBQGMHXBSLYLZ-UHFFFAOYSA-N | [CAS DataBase Reference]
255836-67-0 |
| Hazard Information | Back Directory | [Chemical Properties]
White to pale yellow crystalline powder | [Uses]
2-(Di-tert-butylphosphino)-1,1''-binaphthyl 98% TrixiePhos is a reagent used as ligand in palladium-catalyzed C-O, C-N, and C-C bond forming reactions. |
| Questions And Answer | Back Directory | [Reaction]
- Ligand for the Pd-catalyzed formation of oxygen heterocycles.
- Ligand for the intermolecular Pd-catalyzed synthesis of aryl ethers.
- Ligand for the intramolecular Pd-catalyzed synthesis of aryl ethers.
- Ligand for the synthesis of carbazoles by Pd-catalyzed double N-arylation reaction.
- Ligand for the Pd-catalyzed cyanation of (hetero)arylchlorides.
- Ligand for the Pd-catalyzed intramolecular synthesis of carbazoles via C-H functionalization.
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