5-(Boc-amino)-2-(Boc-aminomethyl)pyridine
≥95%
- Product Code: 69292
CAS:
1456821-59-2
| Molecular Weight: | 323.39 g./mol | Molecular Formula: | C₁₆H₂₅N₃O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26404527 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the preparation of active pharmaceutical ingredients (APIs) and other biologically active molecules. The Boc (tert-butoxycarbonyl) protecting groups in the compound are crucial for safeguarding the amine functionalities during multi-step synthetic processes, ensuring selective reactions and preventing unwanted side reactions. It is often employed in peptide synthesis, where controlled deprotection of the Boc groups allows for the sequential assembly of peptide chains. Additionally, it finds application in the development of small molecule inhibitors and other therapeutic agents, particularly in the fields of oncology and neurology, where precise chemical modifications are essential for optimizing drug efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿16,830.00 |
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| 1.000 | 10-20 days | ฿41,805.00 |
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5-(Boc-amino)-2-(Boc-aminomethyl)pyridine
This chemical is primarily used in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the preparation of active pharmaceutical ingredients (APIs) and other biologically active molecules. The Boc (tert-butoxycarbonyl) protecting groups in the compound are crucial for safeguarding the amine functionalities during multi-step synthetic processes, ensuring selective reactions and preventing unwanted side reactions. It is often employed in peptide synthesis, where controlled deprotection of the Boc groups allows for the sequential assembly of peptide chains. Additionally, it finds application in the development of small molecule inhibitors and other therapeutic agents, particularly in the fields of oncology and neurology, where precise chemical modifications are essential for optimizing drug efficacy and selectivity.
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