(2R,5R)-2,5-Diphenylpyrrolidine
95%
- Product Code: 70875
Alias:
(R,R)-2,5-Diphenylpyrrolidine
CAS:
155155-73-0
| Molecular Weight: | 223.32 g./mol | Molecular Formula: | C₁₆H₁₇N |
|---|---|---|---|
| EC Number: | 680-171-1 | MDL Number: | MFCD07772441 |
| Melting Point: | 50 °C | Boiling Point: | 356.13 °C at 760 mmHg |
| Density: | 1.047±0.06 g/cm3 | Storage Condition: | 2-8°C, protected from light, sealed |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. Its unique stereochemistry makes it valuable in facilitating enantioselective reactions, particularly in the production of pharmaceuticals and fine chemicals. The compound is often employed in metal-catalyzed processes, such as hydrogenation or carbon-carbon bond formation, to achieve high enantiomeric purity in the final products. Additionally, its structural rigidity and ability to induce chirality make it a useful tool in the development of novel catalytic systems for organic synthesis. Researchers also explore its potential in creating chiral materials or as a building block for more complex molecular architectures.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 46-53 |
| Purity (GC) | 95-100% |
| Specific Rotation [α]20/D (c=1, CHCl3) | 105-113 |
| Infrared Spectrometry | Conforms to Structure |
| Note | Low melting point solid; may change state in different environments (solid, liquid, or semi-solid) |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿29,448.00 |
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(2R,5R)-2,5-Diphenylpyrrolidine
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. Its unique stereochemistry makes it valuable in facilitating enantioselective reactions, particularly in the production of pharmaceuticals and fine chemicals. The compound is often employed in metal-catalyzed processes, such as hydrogenation or carbon-carbon bond formation, to achieve high enantiomeric purity in the final products. Additionally, its structural rigidity and ability to induce chirality make it a useful tool in the development of novel catalytic systems for organic synthesis. Researchers also explore its potential in creating chiral materials or as a building block for more complex molecular architectures.
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