(R)-(-)-2-[Hydroxy(diphenyl)methyl]-1-methylpyrrolidine
99%
- Product Code: 60201
Alias:
α,α-Diphenyl-N-methyl-D-prolinol
alpha,alpha-diphenyl-N-methyl-D-prolinol
α,α-Diphenyl-N-methyl-D-prolinol
(R)-α,α-Diphenyl-N-methyl-2-pyrrolidinemethanol
CAS:
144119-12-0
| Molecular Weight: | 267.37 g./mol | Molecular Formula: | C₁₈H₂₁NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00145217 | |
| Melting Point: | 68-71 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This compound is primarily used as a chiral catalyst or resolving agent in asymmetric synthesis, particularly in the pharmaceutical industry. It facilitates the production of enantiomerically pure compounds, which is crucial for developing drugs with specific biological activities. Additionally, it is employed in organic synthesis to induce stereoselectivity in reactions, such as hydrogenation or alkylation processes, ensuring the formation of desired stereoisomers. Its application extends to research laboratories for studying chiral induction and optimizing synthetic pathways for complex molecules.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | WHITE TO YELLOW CRYSTALS TO POWDER AND/OR CHUNKS |
| PURITY | 99-100 |
| MELTING POINT | 70-73 |
| Infrared spectrum | Conforms to Structure |
| SPECIFIC ROTATION A20DC1 CHCL3 | -53 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft17,885.02 |
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| 1.000 | 10-20 days | Ft64,213.68 |
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| 5.000 | 10-20 days | Ft206,054.82 |
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(R)-(-)-2-[Hydroxy(diphenyl)methyl]-1-methylpyrrolidine
This compound is primarily used as a chiral catalyst or resolving agent in asymmetric synthesis, particularly in the pharmaceutical industry. It facilitates the production of enantiomerically pure compounds, which is crucial for developing drugs with specific biological activities. Additionally, it is employed in organic synthesis to induce stereoselectivity in reactions, such as hydrogenation or alkylation processes, ensuring the formation of desired stereoisomers. Its application extends to research laboratories for studying chiral induction and optimizing synthetic pathways for complex molecules.
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