(S)-(−)-α,α-Diphenyl-2-pyrrolidinemethanol
98%
- Product Code: 97454
CAS:
112068-01-6
| Molecular Weight: | 253.34 g./mol | Molecular Formula: | C₁₇H₁₉NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00075506 | |
| Melting Point: | 77-80 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
(S)-(−)-α,α-Diphenyl-2-pyrrolidinemethanol is widely used in asymmetric synthesis as a chiral auxiliary or catalyst. It plays a key role in the production of enantiomerically pure compounds, particularly in pharmaceutical manufacturing, where it helps create drugs with high stereochemical precision. Its application is crucial in the synthesis of complex molecules, such as beta-blockers and other chiral drugs, ensuring enhanced efficacy and reduced side effects. Additionally, it is utilized in academic and industrial research for developing new chiral catalysts and studying stereoselective reactions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | WHITE TO OFF-WHITE POWDER OR CRYSTALS |
| PURITY | 98 100% |
| MELTING POINT | 76-80 |
| Infrared spectrum | Conforms to Structure |
| SOLUBILITY IN CHLOROFORM | ALMOST TRANSPARENCY |
| CHLOROFORM | -65 -69 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿490.00 |
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| 25.000 | 10-20 days | ฿2,160.00 |
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| 100.000 | 10-20 days | ฿8,020.00 |
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(S)-(−)-α,α-Diphenyl-2-pyrrolidinemethanol
(S)-(−)-α,α-Diphenyl-2-pyrrolidinemethanol is widely used in asymmetric synthesis as a chiral auxiliary or catalyst. It plays a key role in the production of enantiomerically pure compounds, particularly in pharmaceutical manufacturing, where it helps create drugs with high stereochemical precision. Its application is crucial in the synthesis of complex molecules, such as beta-blockers and other chiral drugs, ensuring enhanced efficacy and reduced side effects. Additionally, it is utilized in academic and industrial research for developing new chiral catalysts and studying stereoselective reactions.
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