(2S)-1-(11bS)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl-1,2,3,4-tetrahydro-2-methylquinoline
≥98%,≥99% e.e.
- Product Code: 59679
CAS:
1619901-87-9
| Molecular Weight: | 461.5 g./mol | Molecular Formula: | C₃₀H₂₄NO₂P |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 654.3±48.0 °C | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand in catalytic reactions. Its unique structure allows it to effectively induce chirality in the formation of various organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is employed in the development of advanced materials, particularly in the synthesis of chiral polymers and complexes. Its application extends to research in stereoselective transformations, aiding in the creation of enantiomerically pure compounds essential for drug development and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €242.45 |
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(2S)-1-(11bS)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl-1,2,3,4-tetrahydro-2-methylquinoline
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand in catalytic reactions. Its unique structure allows it to effectively induce chirality in the formation of various organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is employed in the development of advanced materials, particularly in the synthesis of chiral polymers and complexes. Its application extends to research in stereoselective transformations, aiding in the creation of enantiomerically pure compounds essential for drug development and material science.
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