A7399712
(S)-(+)-(3,5-Dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)bis[(1S)-1-phenylethyl]amine. , ≥97% , 380230-02-4
Synonym(s):
(+)-N,N-Bis[(1S)-1-phenylethyl]- dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin- 4-amine, (11bR)
| Pack Size | Price | Stock | Quantity |
| 5MG | RMB153.60 | In Stock |
|
| 25MG | RMB394.40 | In Stock |
|
| others | Enquire |
Update time: 2022-07-08
PRODUCT Properties
| Melting point: | 88-89 °C |
| Boiling point: | 710.7±63.0 °C(Predicted) |
| alpha | +13.1° (c 1.01, CHCl3) |
| storage temp. | under inert gas (nitrogen or Argon) at 2-8°C |
| form | Powder |
| pka | -0.57±0.20(Predicted) |
| color | off-white |
| Sensitive | moisture sensitive |
| InChIKey | LKZPDRCMCSBQFN-UIOOFZCWSA-N |
| SMILES | O1C2=CC=C3C(=C2C2=C4C(C=CC=C4)=CC=C2OP1N([C@H](C1=CC=CC=C1)C)[C@H](C1=CC=CC=C1)C)C=CC=C3 |
Description and Uses
The product may be used as a ligand in:
- Iridium-catalyzed allylic etherification of acyclic, achiral allylic carbonates with potassium silanolates to form chiral allylic alcohols.
- Palladium-catalyzed asymmetric allylic cyclisation of N-tosyl and N-benzyl carbonates to form the corresponding pyrrolidine and piperidine derivatives, respectively.
- Intramolecular iridium-catalyzed allylic cyclizationof (E)-allylic methyl carbonates to form 2,5-trans/cis pyrrolidine derivatives.
Safety
| Risk Statements | 36/37/38 |
| Safety Statements | 26-36/37/39 |
| WGK Germany | 3 |

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