[(1,2,5,6-η)-1,5-Cyclooctadiene][(4S)-2-[(5R)-6-(diphenylphosphino-κP)spiro[4.4]nona-1,6-dien-1-yl]-4,5-dihydro-4-(phenylmethyl)oxazole-κN3]-()Iridium(I) Tetrakis[3,5-bis(trifluoromethyl)phenyl]borate
98%
- Product Code: 57547
CAS:
1195511-56-8
| Molecular Weight: | 1623.13 g./mol | Molecular Formula: | C₇₁H₅₀BF₂₄IrNOP |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This complex is primarily used in asymmetric catalysis, particularly in hydrogenation reactions. It is highly effective in producing enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the synthesis of chiral drugs. The compound's unique structure allows it to selectively catalyze the addition of hydrogen to specific substrates, ensuring high enantioselectivity and yield. Additionally, it is employed in the fine chemicals sector for the production of specialty chemicals and intermediates. Its stability and efficiency make it a valuable tool in organic synthesis, especially in processes requiring precise control over stereochemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | $987.56 |
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[(1,2,5,6-η)-1,5-Cyclooctadiene][(4S)-2-[(5R)-6-(diphenylphosphino-κP)spiro[4.4]nona-1,6-dien-1-yl]-4,5-dihydro-4-(phenylmethyl)oxazole-κN3]-()Iridium(I) Tetrakis[3,5-bis(trifluoromethyl)phenyl]borate
This complex is primarily used in asymmetric catalysis, particularly in hydrogenation reactions. It is highly effective in producing enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the synthesis of chiral drugs. The compound's unique structure allows it to selectively catalyze the addition of hydrogen to specific substrates, ensuring high enantioselectivity and yield. Additionally, it is employed in the fine chemicals sector for the production of specialty chemicals and intermediates. Its stability and efficiency make it a valuable tool in organic synthesis, especially in processes requiring precise control over stereochemistry.
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