(S)-1-(tert-Butoxycarbonyl)-2-(4-iodobenzyl)pyrrolidine-2-carboxylic acid
≥95%
- Product Code: 51355
CAS:
1217686-40-2
| Molecular Weight: | 431.27 g./mol | Molecular Formula: | C₁₇H₂₂INO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06796820 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its structure, featuring a pyrrolidine ring and an iodobenzyl group, makes it valuable for constructing molecules with specific stereochemistry and functional groups. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthetic processes. Additionally, the iodine atom provides a handle for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. Its applications are particularly relevant in the development of peptidomimetics and other small molecules targeting therapeutic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,451.00 |
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| 0.250 | 10-20 days | ฿14,796.00 |
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| 1.000 | 10-20 days | ฿37,080.00 |
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(S)-1-(tert-Butoxycarbonyl)-2-(4-iodobenzyl)pyrrolidine-2-carboxylic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its structure, featuring a pyrrolidine ring and an iodobenzyl group, makes it valuable for constructing molecules with specific stereochemistry and functional groups. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthetic processes. Additionally, the iodine atom provides a handle for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. Its applications are particularly relevant in the development of peptidomimetics and other small molecules targeting therapeutic pathways.
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