(R)-tert-Butyl 3-methoxypyrrolidine-1-carboxylate
95%
- Product Code: 37754
CAS:
549532-08-3
| Molecular Weight: | 201.2600 g./mol | Molecular Formula: | C₁₀H₁₉NO₃ |
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| EC Number: | MDL Number: | MFCD16620894 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the development of pharmaceutical agents. Its structure, featuring a pyrrolidine ring and a tert-butyloxycarbonyl (Boc) protecting group, makes it a valuable intermediate in the synthesis of complex molecules. The (R)-configuration of the compound is especially significant in the production of enantiomerically pure drugs, where stereochemistry plays a crucial role in biological activity. It is commonly employed in the preparation of bioactive compounds, including inhibitors, receptor antagonists, and other therapeutic agents targeting neurological and metabolic disorders. Additionally, its methoxy group enhances solubility and reactivity, facilitating its use in various chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $9.72 |
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(R)-tert-Butyl 3-methoxypyrrolidine-1-carboxylate
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the development of pharmaceutical agents. Its structure, featuring a pyrrolidine ring and a tert-butyloxycarbonyl (Boc) protecting group, makes it a valuable intermediate in the synthesis of complex molecules. The (R)-configuration of the compound is especially significant in the production of enantiomerically pure drugs, where stereochemistry plays a crucial role in biological activity. It is commonly employed in the preparation of bioactive compounds, including inhibitors, receptor antagonists, and other therapeutic agents targeting neurological and metabolic disorders. Additionally, its methoxy group enhances solubility and reactivity, facilitating its use in various chemical transformations.
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