(11bS)-2,6-Bis(3,5-dimethylphenyl)-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
98%
- Product Code: 70503
CAS:
1170736-59-0
| Molecular Weight: | 556.6 g./mol | Molecular Formula: | C₃₆H₂₉O₄P |
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| Density: | Storage Condition: | room temperature, dry |
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 dinaphtho[1,3,2]dioxaphosphepin core, makes it effective in promoting enantioselective transformations, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. Additionally, its sterically hindered and electron-rich aromatic groups enhance its ability to stabilize transition states, improving reaction efficiency and selectivity. It is often employed in metal-catalyzed processes, such as hydrogenation or cross-coupling reactions, where high enantiomeric purity is required. Its application extends to the development of novel therapeutic agents and advanced materials with specific chiral properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,511.00 |
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| 0.250 | 10-20 days | ฿6,201.00 |
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| 1.000 | 10-20 days | ฿20,250.00 |
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(11bS)-2,6-Bis(3,5-dimethylphenyl)-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
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 dinaphtho[1,3,2]dioxaphosphepin core, makes it effective in promoting enantioselective transformations, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. Additionally, its sterically hindered and electron-rich aromatic groups enhance its ability to stabilize transition states, improving reaction efficiency and selectivity. It is often employed in metal-catalyzed processes, such as hydrogenation or cross-coupling reactions, where high enantiomeric purity is required. Its application extends to the development of novel therapeutic agents and advanced materials with specific chiral properties.
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