BINOL
| BINOL | |
|---|---|
-_and_(S)-BINOL.svg) | |
| Formula kimikoa | C20H14O2 |
| SMILES kanonikoa | 2D eredua |
| MolView | 3D eredua |
| Mota | konposatu kimiko |
| Ezaugarriak | |
| Fusio-puntua | 217 ℃ |
| Masa molekularra | 286,09938 Da |
| Identifikatzaileak | |
| InChlKey | PPTXVXKCQZKFBN-UHFFFAOYSA-N |
| CAS zenbakia | 602-09-5 |
| ChemSpider | 11269 |
| PubChem | 11762 |
| Gmelin | 189881 |
| ChEMBL | CHEMBL138718 |
| RTECS zenbakia | DU3106000 |
| DSSTox zenbakia | DU3106000 |
| EC zenbakia | 210-014-0 |
| ECHA | 100.009.104 |
| UNII | 25AB254328, 54OT5RRV4C eta M6IDZ128WT |
BINOLa edo 1,1′-Bi-2-naftola a konposatu organiko aromatikoa da C20H14O2 formula duena, alkoholen klasekoa. BINOLak kiralitate axiala du eta ondorioz, bi enantiomero ditu: (S)-BINOLa eta (R)-BINOLa. Solidoa da. Narritagarria eta toxikoa da[1].
BINOLa estekatzaile gisa usatzen da eta enantioselektibitate bikaina erakusten du trantsizio-metalek katalizatutako erreakzio askotan, adibidez hidrogenazio asimetrikoetan.
Erreferentziak
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Index:
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