(11bS)-2,6-Dimethyl-N,N-bis(1-phenylethyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
97%,99%ee
- Product Code: 36166
CAS:
201732-49-2
| Molecular Weight: | 567.6558 g./mol | Molecular Formula: | C₃₈H₃₄NO₂P |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of 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. This is especially valuable in the pharmaceutical industry, where the production of enantiomerically pure compounds is critical for drug development. The compound is often employed as a ligand in transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution, to achieve high enantioselectivity and yield. Its application extends to the synthesis of complex natural products and fine chemicals, where precise control over stereochemistry is essential. Additionally, its stability and robustness under various reaction conditions make it a preferred choice for industrial-scale processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,742.00 |
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(11bS)-2,6-Dimethyl-N,N-bis(1-phenylethyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
This chemical is primarily utilized in the field of 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. This is especially valuable in the pharmaceutical industry, where the production of enantiomerically pure compounds is critical for drug development. The compound is often employed as a ligand in transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution, to achieve high enantioselectivity and yield. Its application extends to the synthesis of complex natural products and fine chemicals, where precise control over stereochemistry is essential. Additionally, its stability and robustness under various reaction conditions make it a preferred choice for industrial-scale processes.
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