2,6-Bis[(2R,4S,5S)-1-benzyl-4,5-diphenylimidazolidin-2-yl]pyridine
90%
- Product Code: 69832
CAS:
1223020-29-8
| Molecular Weight: | 703.9299999999999 g./mol | Molecular Formula: | C₄₉H₄₅N₅ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of enantiomerically pure compounds. Its structure, featuring imidazolidine rings and a central pyridine core, allows it to effectively coordinate with metal centers, enhancing stereoselectivity in various reactions. It is often employed in enantioselective hydrogenation, carbon-carbon bond formation, and other transformations where precise control over chiral induction is critical. Its application is valuable in the pharmaceutical industry for producing chiral drugs and intermediates with high enantiomeric purity. Additionally, it finds use in academic research for developing new catalytic methodologies and exploring stereochemical outcomes in organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 89.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿1,880.00 |
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| 0.050 | 10-20 days | ฿5,310.00 |
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2,6-Bis[(2R,4S,5S)-1-benzyl-4,5-diphenylimidazolidin-2-yl]pyridine
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of enantiomerically pure compounds. Its structure, featuring imidazolidine rings and a central pyridine core, allows it to effectively coordinate with metal centers, enhancing stereoselectivity in various reactions. It is often employed in enantioselective hydrogenation, carbon-carbon bond formation, and other transformations where precise control over chiral induction is critical. Its application is valuable in the pharmaceutical industry for producing chiral drugs and intermediates with high enantiomeric purity. Additionally, it finds use in academic research for developing new catalytic methodologies and exploring stereochemical outcomes in organic synthesis.
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