(S)-(-)-2-Diphenylphosphino-2'-methoxy-1,1'-binaphthyl
98.0%
- Product Code: 68692
CAS:
134484-36-9
| Molecular Weight: | 468.54 g./mol | Molecular Formula: | C₃₃H₂₅OP |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00269686 | |
| Melting Point: | 175-179°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective synthesis, enabling the production of optically active compounds with high selectivity. Its application is prominent in hydrogenation, carbon-carbon bond formation, and other key transformations in organic synthesis. The compound is especially valuable in the pharmaceutical industry for creating chiral intermediates and active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is utilized in academic research to develop novel catalytic processes and study stereochemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,620.00 |
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| 0.500 | 10-20 days | ฿29,990.00 |
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(S)-(-)-2-Diphenylphosphino-2'-methoxy-1,1'-binaphthyl
This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective synthesis, enabling the production of optically active compounds with high selectivity. Its application is prominent in hydrogenation, carbon-carbon bond formation, and other key transformations in organic synthesis. The compound is especially valuable in the pharmaceutical industry for creating chiral intermediates and active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is utilized in academic research to develop novel catalytic processes and study stereochemistry.
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