[2-[(1S)-7'-[BIS[3,5-BIS(TERT-BUTYL)PHENYL]PHOSPHINO-ΚP]-2,2',3,3'-TETRAHYDRO-1,1'-SPIROBI[1H-INDEN]-7-YL]Chemicalbook-4,5-DIHYDROOXAZOLE-ΚN3][(1,2,5,6-Η)-1,5-CYCLOOCTADIENE]-()IRIDIUM(I)TETRAKIS[3,5-BIS(TRIFLUOROMETHYL)PHE
98%
- Product Code: 57568
CAS:
1192772-21-6
| Molecular Weight: | 1861.6 g./mol | Molecular Formula: | C₅₆H₇₂IrNOPC₃₂H₁₂BF₂₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 196 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used as a highly specialized catalyst in asymmetric hydrogenation reactions, particularly in the synthesis of chiral molecules. Its unique structure, featuring a chiral phosphine ligand and an iridium center, makes it highly effective in inducing enantioselectivity, which is crucial for producing pharmaceuticals and fine chemicals with high optical purity. The catalyst is particularly valuable in the production of enantiomerically pure compounds, such as active pharmaceutical ingredients (APIs), where the specific spatial arrangement of atoms is critical for biological activity. Its application extends to organic synthesis, where it facilitates the efficient and selective reduction of unsaturated bonds, such as alkenes and imines, under mild conditions. This contributes to greener and more sustainable chemical processes by reducing waste and improving yield. Additionally, its robustness and stability under reaction conditions make it a preferred choice in industrial and academic research settings for developing novel synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿20,880.00 |
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| 0.050 | 10-20 days | ฿83,080.00 |
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[2-[(1S)-7'-[BIS[3,5-BIS(TERT-BUTYL)PHENYL]PHOSPHINO-ΚP]-2,2',3,3'-TETRAHYDRO-1,1'-SPIROBI[1H-INDEN]-7-YL]Chemicalbook-4,5-DIHYDROOXAZOLE-ΚN3][(1,2,5,6-Η)-1,5-CYCLOOCTADIENE]-()IRIDIUM(I)TETRAKIS[3,5-BIS(TRIFLUOROMETHYL)PHE
This chemical is primarily used as a highly specialized catalyst in asymmetric hydrogenation reactions, particularly in the synthesis of chiral molecules. Its unique structure, featuring a chiral phosphine ligand and an iridium center, makes it highly effective in inducing enantioselectivity, which is crucial for producing pharmaceuticals and fine chemicals with high optical purity. The catalyst is particularly valuable in the production of enantiomerically pure compounds, such as active pharmaceutical ingredients (APIs), where the specific spatial arrangement of atoms is critical for biological activity. Its application extends to organic synthesis, where it facilitates the efficient and selective reduction of unsaturated bonds, such as alkenes and imines, under mild conditions. This contributes to greener and more sustainable chemical processes by reducing waste and improving yield. Additionally, its robustness and stability under reaction conditions make it a preferred choice in industrial and academic research settings for developing novel synthetic pathways.
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