(4S,4''S)-2,2''-(1-Phenylpropane-2,2-diyl)bis(4-phenyl-4,5-dihydrooxazole) (S)-BnPh-SaBOX
95%
- Product Code: 96557
CAS:
1404433-37-9
| Molecular Weight: | 410.51 g./mol | Molecular Formula: | C₂₇H₂₆N₂O₂ |
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| EC Number: | MDL Number: | MFCD27978386 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis reactions. It is highly effective in coordinating with transition metals to form catalysts that facilitate the production of chiral molecules with high enantiomeric purity. Its application is prominent in the synthesis of pharmaceuticals, where the creation of single-enantiomer compounds is crucial for drug efficacy and safety. Additionally, it is employed in organic synthesis for constructing complex molecular architectures with precise stereochemical control, making it valuable in the development of fine chemicals and agrochemicals. Its robust structure and ability to induce high stereoselectivity make it a preferred choice in advanced synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | £132.31 |
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| 1.000 | 10-20 days | £499.72 |
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(4S,4''S)-2,2''-(1-Phenylpropane-2,2-diyl)bis(4-phenyl-4,5-dihydrooxazole) (S)-BnPh-SaBOX
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis reactions. It is highly effective in coordinating with transition metals to form catalysts that facilitate the production of chiral molecules with high enantiomeric purity. Its application is prominent in the synthesis of pharmaceuticals, where the creation of single-enantiomer compounds is crucial for drug efficacy and safety. Additionally, it is employed in organic synthesis for constructing complex molecular architectures with precise stereochemical control, making it valuable in the development of fine chemicals and agrochemicals. Its robust structure and ability to induce high stereoselectivity make it a preferred choice in advanced synthetic methodologies.
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