(S)-2-(Aminomethyl)-1-Boc-pyrrolidine
97%
- Product Code: 66358
Alias:
S-tert-butoxycarbonyl-2-(aminoethyl)pyrrolidine
CAS:
119020-01-8
| Molecular Weight: | 200.28 g./mol | Molecular Formula: | C₁₀H₂₀N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03419257 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is widely used as a chiral building block in the synthesis of pharmaceutical compounds, particularly in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry. Its Boc-protected amino group allows for selective deprotection, making it a valuable intermediate in multi-step organic synthesis. It is often employed in the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas where enantiomeric purity is critical. Additionally, it serves as a precursor in the synthesis of peptidomimetics and other biologically active molecules, enhancing their stability and bioavailability. Its versatility and compatibility with various synthetic methodologies make it a key component in medicinal chemistry research and drug development.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Almost colorless clear liquid |
| PURITY | 96.5-100 |
| Specific rotation a20DC1CHCl3 | -50.0--46.0 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $21.09 |
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| 1.000 | 10-20 days | $58.26 |
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| 5.000 | 10-20 days | $267.20 |
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(S)-2-(Aminomethyl)-1-Boc-pyrrolidine
This chemical is widely used as a chiral building block in the synthesis of pharmaceutical compounds, particularly in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry. Its Boc-protected amino group allows for selective deprotection, making it a valuable intermediate in multi-step organic synthesis. It is often employed in the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas where enantiomeric purity is critical. Additionally, it serves as a precursor in the synthesis of peptidomimetics and other biologically active molecules, enhancing their stability and bioavailability. Its versatility and compatibility with various synthetic methodologies make it a key component in medicinal chemistry research and drug development.
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