Tert-butyl 3-(iodomethyl)pyrrolidine-1-carboxylate
96%
- Product Code: 65087
CAS:
479622-36-1
| Molecular Weight: | 311.16 g./mol | Molecular Formula: | C₁₀H₁₈INO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08059333 | |
| Melting Point: | Boiling Point: | 319°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, away from light, dry, sealed |
Product Description:
This compound is primarily used in organic synthesis as a versatile intermediate for the construction of complex molecules. Its structure, featuring both a tert-butyl ester group and an iodo-methyl substituent, makes it valuable in the development of pharmaceuticals and bioactive compounds. The iodomethyl group serves as a reactive site for further functionalization, enabling coupling reactions or nucleophilic substitutions. Meanwhile, the tert-butyl ester acts as a protecting group for amines, which can be selectively removed under mild acidic conditions. This chemical is particularly useful in the synthesis of pyrrolidine-based compounds, which are common motifs in drug discovery, such as inhibitors, receptor antagonists, and enzyme modulators. Its application extends to the preparation of peptidomimetics and other biologically active molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $40.58 |
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| 0.250 | 10-20 days | $72.70 |
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| 1.000 | 10-20 days | $196.54 |
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Tert-butyl 3-(iodomethyl)pyrrolidine-1-carboxylate
This compound is primarily used in organic synthesis as a versatile intermediate for the construction of complex molecules. Its structure, featuring both a tert-butyl ester group and an iodo-methyl substituent, makes it valuable in the development of pharmaceuticals and bioactive compounds. The iodomethyl group serves as a reactive site for further functionalization, enabling coupling reactions or nucleophilic substitutions. Meanwhile, the tert-butyl ester acts as a protecting group for amines, which can be selectively removed under mild acidic conditions. This chemical is particularly useful in the synthesis of pyrrolidine-based compounds, which are common motifs in drug discovery, such as inhibitors, receptor antagonists, and enzyme modulators. Its application extends to the preparation of peptidomimetics and other biologically active molecules.
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