(R)-(−)-N,N-Dimethyl-1-[(S)-2-(diphenylphosphino)ferrocenyl]ethylamine
≥97%
- Product Code: 68686
Alias:
(R)-(-)-N,N-Dimethyl-1-(2-biphenylphosphino)ferroceneethylamine
CAS:
55700-44-2
| Molecular Weight: | 441.33 g./mol | Molecular Formula: | C₂₆H₂₈FeNP |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00075286 | |
| Melting Point: | 141-143 °C(lit.) | 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. It is highly effective in enantioselective hydrogenation, where it helps in producing chiral compounds with high optical purity. The compound is also employed in asymmetric carbon-carbon bond-forming reactions, such as allylic alkylation and cross-coupling reactions, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Its ferrocene backbone and chiral centers make it a valuable tool in creating complex molecules with specific stereochemistry, essential for drug development and advanced material synthesis.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Yellow to orange to tan solid, powder, or crystals |
| Carbon | 66.5-75% |
| Nitrogen | 2.9-3.4% |
| Infrared Spectrum | Conforms to Structure |
| Purity (HPLC) | 97-100% |
| Specific Rotation [α]20/D (c=2, ethanol) | -330 |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿1,800.00 |
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| 0.500 G | 10-20 days | ฿4,600.00 |
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| 1.000 G | 10-20 days | ฿6,240.00 |
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(R)-(−)-N,N-Dimethyl-1-[(S)-2-(diphenylphosphino)ferrocenyl]ethylamine
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, where it helps in producing chiral compounds with high optical purity. The compound is also employed in asymmetric carbon-carbon bond-forming reactions, such as allylic alkylation and cross-coupling reactions, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Its ferrocene backbone and chiral centers make it a valuable tool in creating complex molecules with specific stereochemistry, essential for drug development and advanced material synthesis.
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