(11bS)-N,N-bis((S)-1-Phenylethyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
97%,99%ee
- Product Code: 51645
CAS:
948309-50-0
| Molecular Weight: | 547.6662 g./mol | Molecular Formula: | C₃₆H₃₈NO₂P |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its unique structure, featuring a chiral phosphine ligand, makes it highly effective in facilitating the formation of chiral centers in organic molecules. It is often employed in transition metal-catalyzed processes, such as hydrogenation, cross-coupling, and allylic substitution reactions, where high enantioselectivity is required. Its application is crucial in the pharmaceutical industry for the production of enantiomerically pure drugs, as well as in the synthesis of fine chemicals and natural products. The compound's ability to induce chirality in reactions enhances the efficiency and specificity of synthetic pathways, making it a valuable tool in advanced organic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft30,641.56 |
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(11bS)-N,N-bis((S)-1-Phenylethyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its unique structure, featuring a chiral phosphine ligand, makes it highly effective in facilitating the formation of chiral centers in organic molecules. It is often employed in transition metal-catalyzed processes, such as hydrogenation, cross-coupling, and allylic substitution reactions, where high enantioselectivity is required. Its application is crucial in the pharmaceutical industry for the production of enantiomerically pure drugs, as well as in the synthesis of fine chemicals and natural products. The compound's ability to induce chirality in reactions enhances the efficiency and specificity of synthetic pathways, making it a valuable tool in advanced organic chemistry.
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