1-[(11bR)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-1,2,3,4-tetrahydroquinoline
98%，ee99%
- Product Code: 39752
CAS:
1360145-09-0
| Molecular Weight: | 447.464241 g./mol | Molecular Formula: | C₂₉H₂₂NO₂P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30187350 | |
| Melting Point: | Boiling Point: | 653.5±48.0 °C | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a tetrahydroquinoline moiety and a dioxaphosphepine ring, makes it effective in facilitating enantioselective transformations. It is commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where high stereochemical control is required. Additionally, it finds application in the development of advanced materials and in research focused on understanding stereochemical outcomes in catalytic processes. Its role in enhancing reaction efficiency and selectivity makes it valuable in both academic and industrial settings.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €77.83 |
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| 0.250 | 10-20 days | €139.56 |
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| 1.000 | 10-20 days | €377.29 |
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1-[(11bR)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-1,2,3,4-tetrahydroquinoline
This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a tetrahydroquinoline moiety and a dioxaphosphepine ring, makes it effective in facilitating enantioselective transformations. It is commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where high stereochemical control is required. Additionally, it finds application in the development of advanced materials and in research focused on understanding stereochemical outcomes in catalytic processes. Its role in enhancing reaction efficiency and selectivity makes it valuable in both academic and industrial settings.
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