(1S,2S)-2-Amino-1-phenylpropyldiphenylphosphine
96%
- Product Code: 122258
CAS:
341968-71-6
| Molecular Weight: | 319.38 g./mol | Molecular Formula: | C₂₁H₂₂NP |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11044864 | |
| Melting Point: | 100-107 ℃ | Boiling Point: | 450.0±38.0 °C(Predicted) |
| Density: | Storage Condition: | Room temperature, dark, inert gas |
Product Description:
This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce optically active compounds with high enantiomeric purity. Its effectiveness stems from its ability to induce chirality in the catalyst, leading to the preferential formation of one enantiomer over the other. This makes it valuable in the pharmaceutical industry for synthesizing chiral drugs and intermediates. Additionally, it is used in academic research to explore new catalytic methodologies and optimize stereoselective reactions.
Product Specification:
| Test | Specification |
|---|---|
| Purity NMR | 96-100 |
| Appearance | Colorless Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿2,691.00 |
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(1S,2S)-2-Amino-1-phenylpropyldiphenylphosphine
This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce optically active compounds with high enantiomeric purity. Its effectiveness stems from its ability to induce chirality in the catalyst, leading to the preferential formation of one enantiomer over the other. This makes it valuable in the pharmaceutical industry for synthesizing chiral drugs and intermediates. Additionally, it is used in academic research to explore new catalytic methodologies and optimize stereoselective reactions.
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