(3R,4R)-tert-Butyl 3-amino-4-methoxypyrrolidine-1-carboxylate
≥95%
- Product Code: 70903
CAS:
1400562-12-0
| Molecular Weight: | 216.28 g./mol | Molecular Formula: | C₁₀H₂₀N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20230534 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both amino and methoxy groups, makes it a valuable building block for the development of drugs targeting neurological and cardiovascular disorders. Specifically, it is often employed in the preparation of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) agents, where its stereochemistry plays a critical role in enhancing drug efficacy and selectivity. Additionally, its tert-butyl carbamate group provides stability during synthetic processes, making it a preferred choice for multi-step organic syntheses.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,403.00 |
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| 0.250 | 10-20 days | ฿22,815.00 |
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(3R,4R)-tert-Butyl 3-amino-4-methoxypyrrolidine-1-carboxylate
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both amino and methoxy groups, makes it a valuable building block for the development of drugs targeting neurological and cardiovascular disorders. Specifically, it is often employed in the preparation of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) agents, where its stereochemistry plays a critical role in enhancing drug efficacy and selectivity. Additionally, its tert-butyl carbamate group provides stability during synthetic processes, making it a preferred choice for multi-step organic syntheses.
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