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| (R)-3,3'-BIS(3,5-BIS(TRIFLUOROMETHYL)PH& Basic information |
Product Name: | (R)-3,3'-BIS(3,5-BIS(TRIFLUOROMETHYL)PH& | Synonyms: | (R)-3,3''-BIS(3,5-BIS(TRIFLUOROMETHYL)PHENYL)-1,1''-BINAPH-2,2''-DIYL HYDRPHOS;(R)-3,3μ-Bis[3,5-bis(trifluoromethyl)phenyl]-1,1μ-bi-2-naphthol cyclic monophosphate, (11bR)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-4-hydroxydinaphtho[2,1-d:1μ,2μ-f]-1,3,2-dioxaphosphepin 4-oxide;(R)-3,3'-Bis[3,5-bis(trifluoroMethyl)phenyl]-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate 95%;(R)-3,3'-Bis[3,5-bis(trifluoromethyl)phenyl]-1,1'-binapthyl-2,2'-diyl hydrogenphosphate;(R)-3,3'-Bis[3,5-bis(trifluoromethyl)phenyl]-1,1'-binaphthalene-;(11BR)-2,6-BIS[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-4-HYDROXY-4-OXIDE-DINAPHTHO[2,1-D:1',2'-F][1,3,2]DIOXAPHOSPHEPIN,98%,(99%EE);2,6-bis(3,5-bis(trifluoromethyl)phenyl)-4-hydroxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide;(R)-3,3'-bis[3,5-Bis(trifluoromethyl)phenyl]-1,1'-binaphthalene-2,2'-diyl hydrogen phosphate | CAS: | 791616-62-1 | MF: | C36H17F12O4P | MW: | 772.47 | EINECS: | | Product Categories: | | Mol File: | 791616-62-1.mol | |
| (R)-3,3'-BIS(3,5-BIS(TRIFLUOROMETHYL)PH& Chemical Properties |
Melting point | 162-175 °C | Boiling point | 722.1±70.0 °C(Predicted) | density | 1.63±0.1 g/cm3(Predicted) | storage temp. | 2-8°C | form | Powder | pka | 1.09±0.20(Predicted) | color | white to light-yellow | optical activity | [α]20/D -220°, c = 1 in chloroform (typical) | InChIKey | DQORDVSQWPKAQJ-UHFFFAOYSA-N |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26 | WGK Germany | 3 | HS Code | 29319090 |
| (R)-3,3'-BIS(3,5-BIS(TRIFLUOROMETHYL)PH& Usage And Synthesis |
Uses | As a chiral Bronsted acid, BINOL- derived cyclic phosphoric acid (such as Akiyama chiral Bronsted acid) was also shown to be an efficient catalyst for the hydrophosphonylation of aldimines at room temperature. | General Description | (R)-3,3′-Bis[3,5-bis(trifluoromethyl)phenyl]-1,1′-binaphthyl-2,2′-diyl hydrogenphosphate is a BINOL-based chiral phosphoric acid, which can efficiently catalyze the nucleophilic addition to imine substrates. [BINOL=1,1′-bi-2-naphthol] |
| (R)-3,3'-BIS(3,5-BIS(TRIFLUOROMETHYL)PH& Preparation Products And Raw materials |
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