(11bR)-N,N-Diisopropyl-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: 36161
CAS:
239113-48-5
| Molecular Weight: | 423.527421 g./mol | Molecular Formula: | C₂₆H₃₄NO₂P |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand in asymmetric catalysis. Its unique structure, featuring a dioxaphosphepine core, makes it highly effective in facilitating enantioselective reactions, which are crucial for producing optically active compounds. These reactions are widely applied in the pharmaceutical industry for the synthesis of chiral drugs, where the specific spatial arrangement of atoms can significantly impact the drug's efficacy and safety. Additionally, it finds use in the development of advanced materials and fine chemicals, where precise control over molecular architecture is essential. Its role in catalysis also extends to academic research, aiding in the exploration of new synthetic methodologies and reaction mechanisms.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $150.95 |
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(11bR)-N,N-Diisopropyl-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand in asymmetric catalysis. Its unique structure, featuring a dioxaphosphepine core, makes it highly effective in facilitating enantioselective reactions, which are crucial for producing optically active compounds. These reactions are widely applied in the pharmaceutical industry for the synthesis of chiral drugs, where the specific spatial arrangement of atoms can significantly impact the drug's efficacy and safety. Additionally, it finds use in the development of advanced materials and fine chemicals, where precise control over molecular architecture is essential. Its role in catalysis also extends to academic research, aiding in the exploration of new synthetic methodologies and reaction mechanisms.
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