(S)-tert-Butyl 3-(2-aminoethyl)pyrrolidine-1-carboxylate
≥95%
- Product Code: 60151
CAS:
274692-08-9
| Molecular Weight: | 214.31 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12828827 | |
| Melting Point: | Boiling Point: | 297.5±13.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring an aminoethyl group and a protected pyrrolidine ring, makes it valuable for constructing complex drug candidates, particularly in the field of central nervous system (CNS) therapeutics. It is often employed in the preparation of compounds targeting receptors or enzymes involved in neurological disorders. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing specificity and reducing potential side effects. The tert-butyloxycarbonyl (Boc) protecting group in its structure facilitates selective reactions during multi-step synthetic processes, making it a versatile building block in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿5,139.00 |
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| 0.100 | 10-20 days | ฿12,861.00 |
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(S)-tert-Butyl 3-(2-aminoethyl)pyrrolidine-1-carboxylate
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring an aminoethyl group and a protected pyrrolidine ring, makes it valuable for constructing complex drug candidates, particularly in the field of central nervous system (CNS) therapeutics. It is often employed in the preparation of compounds targeting receptors or enzymes involved in neurological disorders. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing specificity and reducing potential side effects. The tert-butyloxycarbonyl (Boc) protecting group in its structure facilitates selective reactions during multi-step synthetic processes, making it a versatile building block in medicinal chemistry.
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