(11bS)-8,9,10,11,12,13,14,15-Octahydro-N,N-bis[(1R)-1-phenylethyl]-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
≥98%,≥99% e.e.
- Product Code: 70173
CAS:
479413-76-8
Molecular Weight: | 547.7 g./mol | Molecular Formula: | C₃₆H₃₈NO₂P |
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Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure and stereochemistry make it highly effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals and fine chemicals. The compound is often employed in processes such as hydrogenation, hydroformylation, and cross-coupling reactions, where it helps achieve high enantiomeric purity in the final products. Additionally, its application extends to organic synthesis, where it serves as a key component in the creation of complex molecular architectures with precise stereochemical control.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿4,356.00 |
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(11bS)-8,9,10,11,12,13,14,15-Octahydro-N,N-bis[(1R)-1-phenylethyl]-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure and stereochemistry make it highly effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals and fine chemicals. The compound is often employed in processes such as hydrogenation, hydroformylation, and cross-coupling reactions, where it helps achieve high enantiomeric purity in the final products. Additionally, its application extends to organic synthesis, where it serves as a key component in the creation of complex molecular architectures with precise stereochemical control.
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