(R)-tert-Butyl 3-(iodomethyl)pyrrolidine-1-carboxylate
98%
- Product Code: 82970
CAS:
1187932-69-9
| Molecular Weight: | 311.16 g./mol | Molecular Formula: | C₁₀H₁₈INO₂ |
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| EC Number: | MDL Number: | MFCD08059332 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in pharmaceutical research. Its structure, featuring both a pyrrolidine ring and an iodomethyl group, makes it valuable for introducing functionalized pyrrolidine moieties into target molecules. The iodine atom serves as a reactive site for further transformations, such as cross-coupling reactions, enabling the formation of carbon-carbon bonds. Additionally, the tert-butyloxycarbonyl (Boc) protecting group ensures stability during synthetic processes and can be easily removed when needed. This chemical is often employed in the development of bioactive compounds, including potential drug candidates, where the pyrrolidine scaffold is a key structural element.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,592.00 |
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| 0.250 | 10-20 days | ฿19,530.00 |
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(R)-tert-Butyl 3-(iodomethyl)pyrrolidine-1-carboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in pharmaceutical research. Its structure, featuring both a pyrrolidine ring and an iodomethyl group, makes it valuable for introducing functionalized pyrrolidine moieties into target molecules. The iodine atom serves as a reactive site for further transformations, such as cross-coupling reactions, enabling the formation of carbon-carbon bonds. Additionally, the tert-butyloxycarbonyl (Boc) protecting group ensures stability during synthetic processes and can be easily removed when needed. This chemical is often employed in the development of bioactive compounds, including potential drug candidates, where the pyrrolidine scaffold is a key structural element.
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