R-()-1-Benzyl-3-pyrrolidinol
97%
- Product Code: 71282
Alias:
(R)-1-Benzyl-3-pyrrolidinol, (R)-(+)-N-benzyl-3-hydroxypyrrolidine, (R)-1-benzyl-3-hydroxypyrrolidine
CAS:
101930-07-8
| Molecular Weight: | 177.24 g./mol | Molecular Formula: | C₁₁H₁₅NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00075484 | |
| Melting Point: | Boiling Point: | 116 °C0.9 mm Hg(lit.) | |
| Density: | 1.07 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
R-()-1-Benzyl-3-pyrrolidinol is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the production of various pharmaceuticals. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure compounds, which are crucial for developing drugs with specific therapeutic effects. The compound is often employed in the preparation of intermediates for active pharmaceutical ingredients (APIs), particularly in the creation of molecules that target neurological disorders, cardiovascular diseases, and other medical conditions. Additionally, it finds application in asymmetric catalysis, aiding in the production of complex organic molecules with high enantioselectivity. Its versatility and chiral nature make it a significant component in medicinal chemistry and drug discovery processes.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 97 100% |
| REFRACTIVE INDEX N20D | 1.547-1.55 |
| SPECIFIC GRAVITY 2020C | 1.071-1.074 |
| A20DC5METHANOL | 2.8-4.8 |
| APPEARANCE | COLORLESS TO LIGHT YELLOW OR BROWN LIQUID |
| INFRARED SPECTRUM | CONFORMS |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,920.00 |
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| 5.000 | 10-20 days | ฿6,640.00 |
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| 25.000 | 10-20 days | ฿20,280.00 |
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| 100.000 | 10-20 days | ฿52,880.00 |
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R-()-1-Benzyl-3-pyrrolidinol
R-()-1-Benzyl-3-pyrrolidinol is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the production of various pharmaceuticals. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure compounds, which are crucial for developing drugs with specific therapeutic effects. The compound is often employed in the preparation of intermediates for active pharmaceutical ingredients (APIs), particularly in the creation of molecules that target neurological disorders, cardiovascular diseases, and other medical conditions. Additionally, it finds application in asymmetric catalysis, aiding in the production of complex organic molecules with high enantioselectivity. Its versatility and chiral nature make it a significant component in medicinal chemistry and drug discovery processes.
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