3-(Boc-amino)-3-pyrrolidinecarboxylic Acid
≥95%
- Product Code: 76249
CAS:
869786-49-2
| Molecular Weight: | 230.26 g./mol | Molecular Formula: | C₁₀H₁₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04115498 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical industry. It plays a crucial role in the development of active pharmaceutical ingredients (APIs) and drug candidates. The Boc (tert-butoxycarbonyl) protecting group in the molecule is essential for safeguarding the amine functionality during multi-step synthetic processes, allowing for selective reactions to occur without interference. It is often employed in the production of pyrrolidine-based compounds, which are common structural motifs in drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. Additionally, its carboxylic acid group provides a versatile handle for further chemical modifications, enabling the creation of diverse molecular architectures. Its application extends to peptide synthesis and medicinal chemistry research, where precision in protecting and deprotecting functional groups is critical.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿9,288.00 |
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| 1.000 | 10-20 days | ฿26,712.00 |
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3-(Boc-amino)-3-pyrrolidinecarboxylic Acid
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical industry. It plays a crucial role in the development of active pharmaceutical ingredients (APIs) and drug candidates. The Boc (tert-butoxycarbonyl) protecting group in the molecule is essential for safeguarding the amine functionality during multi-step synthetic processes, allowing for selective reactions to occur without interference. It is often employed in the production of pyrrolidine-based compounds, which are common structural motifs in drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. Additionally, its carboxylic acid group provides a versatile handle for further chemical modifications, enabling the creation of diverse molecular architectures. Its application extends to peptide synthesis and medicinal chemistry research, where precision in protecting and deprotecting functional groups is critical.
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