Methyl 2-((tert-butoxycarbonyl)(methyl)amino)acetate
≥95%
- Product Code: 41170
CAS:
42492-57-9
| Molecular Weight: | 203.24 g./mol | Molecular Formula: | C₉H₁₇NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04973115 | |
| Melting Point: | Boiling Point: | 249.6°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, where it aids in the protection of amino groups during multi-step reactions. The tert-butoxycarbonyl (Boc) group acts as a protective moiety, ensuring selective reactivity in the presence of other functional groups. Additionally, it is employed in the development of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that require controlled introduction of nitrogen-containing structures. Its ester functionality also makes it a versatile precursor for further chemical modifications, such as hydrolysis or reduction, to yield desired products for various applications in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿333.00 |
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| 1.000 | 10-20 days | ฿531.00 |
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| 5.000 | 10-20 days | ฿2,178.00 |
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| 25.000 | 10-20 days | ฿9,162.00 |
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Methyl 2-((tert-butoxycarbonyl)(methyl)amino)acetate
This compound is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, where it aids in the protection of amino groups during multi-step reactions. The tert-butoxycarbonyl (Boc) group acts as a protective moiety, ensuring selective reactivity in the presence of other functional groups. Additionally, it is employed in the development of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that require controlled introduction of nitrogen-containing structures. Its ester functionality also makes it a versatile precursor for further chemical modifications, such as hydrolysis or reduction, to yield desired products for various applications in medicinal chemistry and drug discovery.
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