Methyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate
98%
- Product Code: 76485
CAS:
889670-02-4
| Molecular Weight: | 329.13 g./mol | Molecular Formula: | C₉H₁₆INO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20231367 | |
| Melting Point: | Boiling Point: | 356.5 °C at 760 mmHg (lit.) | |
| Density: | Storage Condition: | −20°C, inert gas, dark, frozen |
Product Description:
This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in peptide synthesis, where it serves as a building block for introducing specific amino acid structures into peptides. The tert-butoxycarbonyl (Boc) group acts as a protective group for the amine functionality, allowing selective reactions to occur at other sites of the molecule. The iodine atom provides a reactive site for further functionalization, such as cross-coupling reactions, which are essential in the development of pharmaceuticals and bioactive compounds. Its application is crucial in the production of targeted drugs and research chemicals, enabling the creation of structurally diverse and biologically active molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $108.28 |
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Methyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate
This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in peptide synthesis, where it serves as a building block for introducing specific amino acid structures into peptides. The tert-butoxycarbonyl (Boc) group acts as a protective group for the amine functionality, allowing selective reactions to occur at other sites of the molecule. The iodine atom provides a reactive site for further functionalization, such as cross-coupling reactions, which are essential in the development of pharmaceuticals and bioactive compounds. Its application is crucial in the production of targeted drugs and research chemicals, enabling the creation of structurally diverse and biologically active molecules.
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