| Identification | Back Directory | [Name]
(R)-3,3'-BIS(TRIPHENYLSILYL)-1,1'-BI-2-& | [CAS]
111822-69-6 | [Synonyms]
(R)-3,3'-BIS(TRIPHENYLSILYL)-1,1'-BI-2-&
(R)-3,3μ-Bis(triphenylsilyl)-1,1μ-bi-2-naphthol
(R)-3,3'-Bis(triphenylsilyl)-1,1'-bi-2-naphthol 96%
(R)-(+)-3,3'-Bis(triphenylsilyl)-1,1'-bi-2,2'-naphthol
(R)-3,3'-Bis(triphenylsilyl)-1,1'-bi-2-naphthol, 99%e.e.
(R)-3,3μ-Bis(triphenylsilyl)-1,1μ-binaphthalene-2,2μ-diol
(1R)-3,3'- bis (triphenylsilyl) [1,1'- binaphthyl ]-2,2'- diol
[1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)-, (1R)- | [Molecular Formula]
C56H42O2Si2 | [MDL Number]
MFCD09265078 | [MOL File]
111822-69-6.mol | [Molecular Weight]
803.1 |
| Chemical Properties | Back Directory | [Melting point ]
103-145 °C | [density ]
1.27±0.1 g/cm3(Predicted) | [pka]
8.06±0.50(Predicted) | [optical activity]
[α]20/D +114°, c = 1 in chloroform |
| Hazard Information | Back Directory | [Chemical Properties]
White powder | [Uses]
Precursor to a chiral Bronsted acid (674745) used to catalyze an enantioselective aza Diels-Alder reaction providing bicyclic lactams. Rare earth metal complexes of this chiral binapthol catalyze an intramolecular hydroamination of amino olefins leading to chiral pyrrolidines. |
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