N-[(1S)-2'-amino-4,4',6,6'-tetrakis(trifluoromethyl)[1,1'-biphenyl]-2-yl]-P,P-diphenyl-Phosphinous amide
98%
- Product Code: 70703
CAS:
1093238-10-8
Molecular Weight: | 640.4025794 g./mol | Molecular Formula: | C₂₈H₁₇F₁₂N₂P |
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Density: | Storage Condition: | 2-8°C |
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 trifluoromethyl groups and a biphenyl backbone, enhances its ability to induce chirality in the synthesis of complex molecules. It is often employed in the production of pharmaceuticals, where the creation of enantiomerically pure compounds is crucial for drug efficacy and safety. Additionally, its phosphinous amide moiety makes it valuable in transition metal catalysis, facilitating reactions such as hydrogenation, cross-coupling, and C-H activation. The compound's stability and selectivity make it a preferred choice in the development of advanced materials and fine chemicals.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.010 | 10-20 days | ฿3,042.00 |
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0.050 | 10-20 days | ฿12,204.00 |
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N-[(1S)-2'-amino-4,4',6,6'-tetrakis(trifluoromethyl)[1,1'-biphenyl]-2-yl]-P,P-diphenyl-Phosphinous amide
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 trifluoromethyl groups and a biphenyl backbone, enhances its ability to induce chirality in the synthesis of complex molecules. It is often employed in the production of pharmaceuticals, where the creation of enantiomerically pure compounds is crucial for drug efficacy and safety. Additionally, its phosphinous amide moiety makes it valuable in transition metal catalysis, facilitating reactions such as hydrogenation, cross-coupling, and C-H activation. The compound's stability and selectivity make it a preferred choice in the development of advanced materials and fine chemicals.
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