(3S,4S)-tert-Butyl 3-(benzylamino)-4-hydroxypyrrolidine-1-carboxylate
95%
- Product Code: 36780
CAS:
252574-03-1
| Molecular Weight: | 292.3734 g./mol | Molecular Formula: | C₁₆H₂₄N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11109734 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Its structure, featuring both a pyrrolidine ring and a benzylamino group, makes it valuable for designing molecules that interact with biological targets, such as enzymes or receptors. Additionally, it is employed in the preparation of chiral compounds, leveraging its stereochemistry to achieve high enantioselectivity in asymmetric synthesis. Its tert-butyl ester group also provides stability during chemical reactions, making it a versatile building block in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,733.00 |
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(3S,4S)-tert-Butyl 3-(benzylamino)-4-hydroxypyrrolidine-1-carboxylate
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Its structure, featuring both a pyrrolidine ring and a benzylamino group, makes it valuable for designing molecules that interact with biological targets, such as enzymes or receptors. Additionally, it is employed in the preparation of chiral compounds, leveraging its stereochemistry to achieve high enantioselectivity in asymmetric synthesis. Its tert-butyl ester group also provides stability during chemical reactions, making it a versatile building block in medicinal chemistry.
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