(R)-tert-Butyl 3-iodopyrrolidine-1-carboxylate
≥95%
- Product Code: 113567
CAS:
1234576-86-3
| Molecular Weight: | 297.13 g./mol | Molecular Formula: | C₉H₁₆INO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17015908 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a pyrrolidine ring with an iodine substituent, makes it a valuable intermediate in the construction of complex organic compounds. The iodine atom serves as a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the introduction of diverse chemical groups. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances stability during synthetic processes and can be selectively removed under mild conditions, allowing for further modifications. This compound is often employed in the synthesis of chiral molecules, contributing to the production of enantiomerically pure drugs and other biologically active compounds. Its versatility and reactivity make it a key building block in medicinal chemistry and drug discovery research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿6,615.00 |
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(R)-tert-Butyl 3-iodopyrrolidine-1-carboxylate
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a pyrrolidine ring with an iodine substituent, makes it a valuable intermediate in the construction of complex organic compounds. The iodine atom serves as a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the introduction of diverse chemical groups. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances stability during synthetic processes and can be selectively removed under mild conditions, allowing for further modifications. This compound is often employed in the synthesis of chiral molecules, contributing to the production of enantiomerically pure drugs and other biologically active compounds. Its versatility and reactivity make it a key building block in medicinal chemistry and drug discovery research.
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