(11bR)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
≥98%,99%e.e.
- Product Code: 70340
CAS:
791616-62-1
| Molecular Weight: | 772.5 g./mol | Molecular Formula: | C₃₆H₁₇F₁₂O₄P |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 162-167°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of enantiomerically pure compounds. Its unique structure, featuring trifluoromethyl groups, enhances its electron-withdrawing properties, making it highly effective in facilitating challenging transformations. It is often employed in metal-catalyzed reactions, such as hydrogenation, where it helps achieve high enantioselectivity. Additionally, its stability and robustness under various reaction conditions make it a valuable tool in pharmaceutical research and development, especially in the production of chiral drugs. The compound’s ability to induce asymmetry in organic molecules is critical for creating biologically active compounds with high precision.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Light Yellow and Faint Beige to Beige Crystal to Powder |
| PURITY | 98 |
| CHLOROFORM | -255.0 -205.0 |
| MELTING POINT | 160-180 |
| PURITY ee | 99 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $67.64 |
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| 0.100 | 10-20 days | $187.19 |
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| 0.250 | 10-20 days | $373.60 |
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| 1.000 | 10-20 days | $935.96 |
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(11bR)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of enantiomerically pure compounds. Its unique structure, featuring trifluoromethyl groups, enhances its electron-withdrawing properties, making it highly effective in facilitating challenging transformations. It is often employed in metal-catalyzed reactions, such as hydrogenation, where it helps achieve high enantioselectivity. Additionally, its stability and robustness under various reaction conditions make it a valuable tool in pharmaceutical research and development, especially in the production of chiral drugs. The compound’s ability to induce asymmetry in organic molecules is critical for creating biologically active compounds with high precision.
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