(S)-()-N,N-Dimethyl-1-(2-diphenylphosphino)ferrocenylethyla
97%
- Product Code: 68689
Alias:
(S)-(+)-N,N-Dimethyl-1-(2-biphenylphosphino)ferroceneethylamine
CAS:
55650-58-3
| Molecular Weight: | 441.34 g./mol | Molecular Formula: | C₂₆H₂₈FeNP |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00075285 | |
| Melting Point: | 141-143°C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its application is significant in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with high specificity and reduced side effects. The compound is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. Its ferrocene backbone and diphenylphosphino group provide excellent stability and selectivity, making it a valuable tool in organic synthesis for creating complex molecules with precise stereochemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light Yellow to Brown Powder to Crystal |
| PURITY | 96.5-100 |
| Proton NMR spectrum | Conforms to Structure |
| Infrared spectrum | Conforms to Structure |
| Specific rotation a20DC2ethanol | -330 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,750.00 |
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| 0.500 | 10-20 days | ฿7,570.00 |
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(S)-()-N,N-Dimethyl-1-(2-diphenylphosphino)ferrocenylethyla
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its application is significant in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with high specificity and reduced side effects. The compound is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. Its ferrocene backbone and diphenylphosphino group provide excellent stability and selectivity, making it a valuable tool in organic synthesis for creating complex molecules with precise stereochemistry.
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