Nameracemic-2,2'-Bis(diphenylphosphino)-1,1'-binaphthylSynonymsBINAPBinap(?-Binap1.1'-Binaphthyl-2.2
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| Nome | racemic-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl |
| Sinonimi | BINAP Binap (?-Binap 1.1'-Binaphthyl-2.2'-Diphemyl Phosphine 2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL (?-2,2-Bis(Diphenylphosphino)-1,1-Binaphthyl Rac-2,2-Bis(Diphenylphosphino)-1,1-Binaphthyl 2,2'-Bis(diphenylphosphino)-1,1'-binaphthalene Racemic-2,2'-bis(diphenylphosphino)-1,1'-binaphthy racemic-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl S(-)-(1,1'-Binaphthalene-2,2'-Diyl)Bis(Diphenylphosphine) RACEMIC-2,2''-BIS(DIPHENYLPHOSPHINO)-1,1''-BINAPHTHYL BINAP 2,2'-Bis-(diphenylphosphino)-1,1'-binaphthyl (Racemic BINAP) |
| CAS | 98327-87-8 |
| EINECS | 619-338-0 |
| InChIKey | MUALRAIOVNYAIW-UHFFFAOYSA-N |
| Formula molecolare | C44H32P2 |
| massa molare | 622.69 |
| Punto di fusione | 283-286°C(lit.) |
| punto Boling | 724.3±55.0 °C(Predicted) |
| Solubilità in acqua | Soluble in tetrahydrofuran, benzene and dichloromethane. Slightly soluble in ether, methanol and ethanol. Insoluble in water. |
| Solubilità | Chloroform (Slightly, Sonicated), Dichloromethane (Slightly, Heated), |
| Aspetto | White to beige powder |
| Colore | White to light beige |
| Merck | 14,1223 |
| BRN | 5321443 |
| Condizioni di conservazione | Keep in dark place,Inert atmosphere,Room temperature |
| Sensibile | Air Sensitive |
| MDL | MFCD00010805 |
| Proprietà fisiche e chimiche | Melting point 280-285°C. |
| Utilizzo | Used for asymmetric hydrogenation catalysis, carbonyl reduction, etc. A ligand for the palladium-catalyzed arylamine coupling reaction for the preparation of desmethylthio-colchicine? cicatine. It can be used in combination with Cu(II) to catalyze the addition reaction of arylsulfonamide to producUsed for asymmetric hydrogenation catalysis, carbonyl reduction, etc. A ligand for the palladium-catalyzed arylamine coupling reaction for the preparation of desmethylthio-colchicine? cicatine. It can be used in combination with Cu(II) to catalyze the addition reaction of arylsulfonamide to produce styrene and olefins. It can also be used for palladium-catalyzed tripyridyl amine reaction.e styrene and olefins. It can also be used for palladium-catalyzed tripyridyl amine reaction. |
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