(S,S)-DACH-naphthyl trost ligand
95%
- Product Code: 126679
Alias:
(1S,2S)-(-)-1,2-diaminocyclohexane-N,N'-bis(2-diphenylphosphine-1-naphthoyl);(1S,2S)-(-)- N,N'-bis(2-diphenylphosphino-1-naphthoyl)-1,2-cyclohexanediamine
CAS:
205495-66-5
| Molecular Weight: | 790.87 g./mol | Molecular Formula: | C₅₂H₄₄N₂O₂P₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02684552 | |
| Melting Point: | 232-237 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
The (S,S)-DACH-naphthyl trost ligand is primarily utilized in asymmetric synthesis, particularly in catalytic asymmetric reactions. It is highly effective in facilitating enantioselective transformations, such as the Trost asymmetric allylic alkylation, which is crucial for producing chiral intermediates in pharmaceutical and fine chemical synthesis. Its application extends to the synthesis of complex organic molecules, including natural products and bioactive compounds, where high enantiomeric purity is essential. The ligand's ability to induce chirality in metal-catalyzed reactions makes it a valuable tool in the development of enantioselective processes in both academic research and industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Brown Powder Or Crystal Or Chunk(s) |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $48.06 |
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| 1.000 | 10-20 days | $186.32 |
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(S,S)-DACH-naphthyl trost ligand
The (S,S)-DACH-naphthyl trost ligand is primarily utilized in asymmetric synthesis, particularly in catalytic asymmetric reactions. It is highly effective in facilitating enantioselective transformations, such as the Trost asymmetric allylic alkylation, which is crucial for producing chiral intermediates in pharmaceutical and fine chemical synthesis. Its application extends to the synthesis of complex organic molecules, including natural products and bioactive compounds, where high enantiomeric purity is essential. The ligand's ability to induce chirality in metal-catalyzed reactions makes it a valuable tool in the development of enantioselective processes in both academic research and industrial applications.
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