N-[(1S)-1-[1,1''-Biphenyl]-2-yl-2-(diphenylphosphino)ethyl]-3,5-bis(trifluoromethyl)-benzamide
95%
- Product Code: 64935
CAS:
2089424-10-0
| Molecular Weight: | 621.55 g./mol | Molecular Formula: | C₃₅H₂₆F₆NOP |
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| EC Number: | MDL Number: | MFCD32697228 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral molecules. Its unique structure, featuring a diphenylphosphino group and trifluoromethyl substituents, makes it an effective ligand in transition metal-catalyzed reactions. It is often employed in hydrogenation, cross-coupling, and other enantioselective transformations, enabling the production of optically active compounds with high selectivity. This is especially valuable in the pharmaceutical industry for the synthesis of chiral drugs and intermediates. Additionally, its robust steric and electronic properties enhance catalytic efficiency and stability in complex reaction environments.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.005 | 10-20 days | $105.83 |
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| 0.025 | 10-20 days | $353.58 |
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| 0.100 | 10-20 days | $1,203.02 |
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N-[(1S)-1-[1,1''-Biphenyl]-2-yl-2-(diphenylphosphino)ethyl]-3,5-bis(trifluoromethyl)-benzamide
This compound is primarily utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral molecules. Its unique structure, featuring a diphenylphosphino group and trifluoromethyl substituents, makes it an effective ligand in transition metal-catalyzed reactions. It is often employed in hydrogenation, cross-coupling, and other enantioselective transformations, enabling the production of optically active compounds with high selectivity. This is especially valuable in the pharmaceutical industry for the synthesis of chiral drugs and intermediates. Additionally, its robust steric and electronic properties enhance catalytic efficiency and stability in complex reaction environments.
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