N-Boc-4-oxo-L-proline methyl ester
97%
- Product Code: 58024
CAS:
102195-80-2
| Molecular Weight: | 243.26 g./mol | Molecular Formula: | C₁₁H₁₇NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861778 | |
| Melting Point: | 35-40°C | Boiling Point: | |
| Density: | Storage Condition: | -20°C |
Product Description:
N-Boc-4-oxo-L-proline methyl ester is widely used in organic synthesis, particularly in the production of peptides and pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, enabling the introduction of the proline moiety into target compounds. Its Boc-protecting group ensures selective reactivity during multi-step reactions, making it valuable in the construction of peptidomimetics and bioactive molecules. Additionally, it is employed in the development of protease inhibitors and other therapeutic agents, leveraging its structural features to enhance drug stability and efficacy. Its versatility also extends to the synthesis of natural products and chiral compounds, where precise control over stereochemistry is essential.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white to brown powder |
| PURITY | 96.5-100 |
| MELTING POINT | 39-46 |
| Infrared spectrum | Conforms to Structure |
| Specific rotation a20Dc 1chloroform | 11 |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿290.00 |
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| 1.000 | 10-20 days | ฿590.00 |
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| 5.000 | 10-20 days | ฿980.00 |
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| 25.000 | 10-20 days | ฿3,820.00 |
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N-Boc-4-oxo-L-proline methyl ester
N-Boc-4-oxo-L-proline methyl ester is widely used in organic synthesis, particularly in the production of peptides and pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, enabling the introduction of the proline moiety into target compounds. Its Boc-protecting group ensures selective reactivity during multi-step reactions, making it valuable in the construction of peptidomimetics and bioactive molecules. Additionally, it is employed in the development of protease inhibitors and other therapeutic agents, leveraging its structural features to enhance drug stability and efficacy. Its versatility also extends to the synthesis of natural products and chiral compounds, where precise control over stereochemistry is essential.
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