((S)-1-((S)-1-Phenylethyl)pyrrolidin-3-yl)methanol
≥95%
- Product Code: 70760
CAS:
173724-95-3
| Molecular Weight: | 205.30 g./mol | Molecular Formula: | C₁₃H₁₉NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15526584 | |
| Melting Point: | Boiling Point: | 281.1±15.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block or intermediate in the production of pharmaceuticals. Its structure, featuring a pyrrolidine ring and a phenylethyl group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the synthesis of enantiomerically pure drugs, where the stereochemical configuration plays a critical role in biological activity. Additionally, it can serve as a ligand or catalyst in asymmetric synthesis, aiding in the creation of chiral compounds with high enantioselectivity. Its applications extend to research and development in medicinal chemistry, where it is used to explore new drug candidates or optimize existing therapeutic agents.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,580.00 |
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| 0.250 | 10-20 days | ฿11,120.00 |
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((S)-1-((S)-1-Phenylethyl)pyrrolidin-3-yl)methanol
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block or intermediate in the production of pharmaceuticals. Its structure, featuring a pyrrolidine ring and a phenylethyl group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the synthesis of enantiomerically pure drugs, where the stereochemical configuration plays a critical role in biological activity. Additionally, it can serve as a ligand or catalyst in asymmetric synthesis, aiding in the creation of chiral compounds with high enantioselectivity. Its applications extend to research and development in medicinal chemistry, where it is used to explore new drug candidates or optimize existing therapeutic agents.
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