(R,R)-DACH-naphthyl trost ligand
95%
- Product Code: 126678
Alias:
(1R,2R)-(+)-1,2-diaminocyclohexane-N,N'-bis(2-phenylphosphine-1-naphthoyl);(1R,2R)-(-)-N ,N'-bis(2-diphenylphosphino-1-naphthoyl)-1,2-cyclohexanediamine
CAS:
174810-09-4
| Molecular Weight: | 790.87 g./mol | Molecular Formula: | C₅₂H₄₄N₂O₂P₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02684551 | |
| Melting Point: | 224-231 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
The (R,R)-DACH-naphthyl Trost ligand is widely used in asymmetric catalysis, particularly in enantioselective synthesis. It plays a crucial role in facilitating carbon-carbon bond-forming reactions, such as allylic alkylations and other transition metal-catalyzed processes. Its application is prominent in the pharmaceutical industry, where it aids in the production of chiral molecules with high enantiomeric purity, essential for active pharmaceutical ingredients (APIs). Additionally, it is employed in academic research to develop novel synthetic methodologies for complex organic compounds. The ligand’s ability to induce high stereoselectivity makes it a valuable tool in the synthesis of natural products and fine chemicals.
Product Specification:
| Test | Specification |
|---|---|
| Carbon | 74.2-83.7 |
| Nitrogen | 3.2-3.8 |
| Purity (HPLC) | 95-100 |
| Specific Rotation | 63-75 |
| Specific Rotation | 63-75 |
| Appearance | White To Tan Powder |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €91.28 |
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| 1.000 | 10-20 days | €275.96 |
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(R,R)-DACH-naphthyl trost ligand
The (R,R)-DACH-naphthyl Trost ligand is widely used in asymmetric catalysis, particularly in enantioselective synthesis. It plays a crucial role in facilitating carbon-carbon bond-forming reactions, such as allylic alkylations and other transition metal-catalyzed processes. Its application is prominent in the pharmaceutical industry, where it aids in the production of chiral molecules with high enantiomeric purity, essential for active pharmaceutical ingredients (APIs). Additionally, it is employed in academic research to develop novel synthetic methodologies for complex organic compounds. The ligand’s ability to induce high stereoselectivity makes it a valuable tool in the synthesis of natural products and fine chemicals.
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