(11aR)-N,N-Bis((S)-1-phenylethyl)-4,5,6,7-tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-amine
98%
- Product Code: 36152
CAS:
656233-47-5
| Molecular Weight: | 505.5900 g./mol | Molecular Formula: | C₃₃H₃₂NO₂P |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal catalysts. Its unique structure, featuring a phosphocin core and chiral phenylethyl groups, makes it highly effective in facilitating enantioselective reactions. These reactions are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals, where the specific spatial arrangement of atoms (chirality) can significantly impact the biological activity and efficacy of the final product. Additionally, its application extends to the study of stereochemistry and the development of novel catalytic systems for organic transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $217.32 |
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(11aR)-N,N-Bis((S)-1-phenylethyl)-4,5,6,7-tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-amine
This chemical is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal catalysts. Its unique structure, featuring a phosphocin core and chiral phenylethyl groups, makes it highly effective in facilitating enantioselective reactions. These reactions are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals, where the specific spatial arrangement of atoms (chirality) can significantly impact the biological activity and efficacy of the final product. Additionally, its application extends to the study of stereochemistry and the development of novel catalytic systems for organic transformations.
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