3-Amino-1-(tert-butoxycarbonyl)piperidine-3-carboxylic acid
98%
- Product Code: 39702
CAS:
368866-17-5
| Molecular Weight: | 244.2900 g./mol | Molecular Formula: | C₁₁H₂₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03790945 | |
| Melting Point: | Boiling Point: | 394.737 °C at 760 mmHg | |
| Density: | 1.332g/cm3 | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of peptidomimetics and active pharmaceutical ingredients (APIs). Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it a valuable intermediate in organic synthesis. It is commonly employed in peptide coupling reactions, where the Boc group ensures selective protection of the amino group during multi-step synthesis. Additionally, it serves as a building block in the creation of complex molecules, including those with potential therapeutic applications in neurological and metabolic disorders. Its versatility in medicinal chemistry highlights its importance in drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,871.00 |
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3-Amino-1-(tert-butoxycarbonyl)piperidine-3-carboxylic acid
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of peptidomimetics and active pharmaceutical ingredients (APIs). Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it a valuable intermediate in organic synthesis. It is commonly employed in peptide coupling reactions, where the Boc group ensures selective protection of the amino group during multi-step synthesis. Additionally, it serves as a building block in the creation of complex molecules, including those with potential therapeutic applications in neurological and metabolic disorders. Its versatility in medicinal chemistry highlights its importance in drug discovery and development processes.
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