(S)-3-((tert-Butoxycarbonyl)amino)-3-(6-methoxypyridin-3-yl)propanoic acid
95%
- Product Code: 38387
CAS:
1217755-81-1
| Molecular Weight: | 296.3190 g./mol | Molecular Formula: | C₁₄H₂₀N₂O₅ |
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| EC Number: | MDL Number: | MFCD04118073 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxypyridine moiety, makes it a valuable intermediate in organic synthesis. The Boc group is often employed to protect amines during multi-step reactions, ensuring selective transformations. The methoxypyridine component can contribute to the biological activity of the final drug molecule, potentially enhancing binding affinity or modulating pharmacokinetic properties. It is commonly utilized in the preparation of compounds targeting neurological disorders, inflammation, or other therapeutic areas where pyridine derivatives play a role. Additionally, its chiral center allows for the creation of enantiomerically pure drugs, which is critical for ensuring efficacy and reducing side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿14,940.00 |
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(S)-3-((tert-Butoxycarbonyl)amino)-3-(6-methoxypyridin-3-yl)propanoic acid
This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxypyridine moiety, makes it a valuable intermediate in organic synthesis. The Boc group is often employed to protect amines during multi-step reactions, ensuring selective transformations. The methoxypyridine component can contribute to the biological activity of the final drug molecule, potentially enhancing binding affinity or modulating pharmacokinetic properties. It is commonly utilized in the preparation of compounds targeting neurological disorders, inflammation, or other therapeutic areas where pyridine derivatives play a role. Additionally, its chiral center allows for the creation of enantiomerically pure drugs, which is critical for ensuring efficacy and reducing side effects.
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