Methyl (2S,4S)-1-Boc-4-aminopyrrolidine-2-carboxylate
≥95%
- Product Code: 76150
CAS:
121148-01-4
| Molecular Weight: | 244.29 g./mol | Molecular Formula: | C₁₁H₂₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861781 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is widely used in the synthesis of pharmaceuticals, particularly in the development of peptidomimetics and protease inhibitors. Its structure, featuring both a Boc-protected amine and a carboxylate ester, makes it a versatile intermediate in organic synthesis. It is often employed in the construction of complex molecules, especially in the field of medicinal chemistry, where it serves as a building block for creating biologically active compounds. The stereochemistry of the molecule is crucial for its application in enantioselective synthesis, ensuring the production of specific stereoisomers with desired biological activity. Additionally, it is utilized in the preparation of chiral ligands and catalysts, which are essential in asymmetric synthesis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to yellow liquid |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿16,310.00 |
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| 5.000 | 10-20 days | ฿55,760.00 |
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Methyl (2S,4S)-1-Boc-4-aminopyrrolidine-2-carboxylate
This compound is widely used in the synthesis of pharmaceuticals, particularly in the development of peptidomimetics and protease inhibitors. Its structure, featuring both a Boc-protected amine and a carboxylate ester, makes it a versatile intermediate in organic synthesis. It is often employed in the construction of complex molecules, especially in the field of medicinal chemistry, where it serves as a building block for creating biologically active compounds. The stereochemistry of the molecule is crucial for its application in enantioselective synthesis, ensuring the production of specific stereoisomers with desired biological activity. Additionally, it is utilized in the preparation of chiral ligands and catalysts, which are essential in asymmetric synthesis.
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